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[Report]

Pipeline Insight: Molecular Targeted Cancer Therapies - Can anything else revolutionize the market?

Published: 2007/10

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Description

Table of Contents

  • ABOUT DATAMONITOR HEALTHCARE
    • About the Oncology pharmaceutical analysis team
  • CHAPTER 1 EXECUTIVE SUMMARY
    • Scope of analysis
    • Datamonitor insight into the molecular targeted therapies market
    • Related reports
    • Upcoming reports
  • CHAPTER 2 PIPELINE OVERVIEW AND DYNAMICS
    • Pipeline overview
      • Late-phase pipeline molecular targeted cancer therapies
      • Phase II pipeline molecular targeted cancer therapies
      • Phase I pipeline molecular targeted cancer therapies
    • Pipeline by developmental phase and class of drug
      • There are 329 different MTTs in the clinical development pipeline
        • The cell cycle and apoptosis targeted agents make up the largest number of MTTs in the pipeline
      • Segmentation of drugs by developmental phase reflects attrition rate of drug development in the oncology market
        • Targeted therapy remains a promising anticancer drug development strategy
        • Developmental agents by phase for each class
    • Pipeline by indication
      • Pipeline MTTs are being investigated in 29 different cancers
        • The ' big four' tumor types are the most popular indications for development
    • Pipeline by mode of action
      • Pipeline products are directed against a huge variety and combination of molecular targets
      • The VEGF/VEGFR family remains the focus of development for MTTs
    • Pipeline by company
      • There are 175 different companies developing targeted therapies
        • Developmental pipeline dominated by small pharma/biotech players
      • There are 19 companies with MTT products in late-phase development
      • Top three companies in terms of number of pipeline MTT products are Pfizer, AstraZeneca and Novartis
        • Pfizer - 21 MTT pipeline products
        • AstraZeneca - 15 MTT pipeline products
        • Novartis - 12 MTT pipeline products
    • Key metrics
    • Datamonitor pipeline assessment summary
  • CHAPTER 3 CURRENT MARKET STATUS & PIPELINE CLASSIFICATION
    • Targeted therapies overview
      • The development of molecular targeted therapies
        • Current therapies are less cancer cell-specific
        • The strategy is to target the specific survival factors of a tumor
        • Key issue is the identification of targets unique to cancer cells
    • Market definition
      • L1X3 - Antineoplastic monoclonal antibodies
      • L1X9 - All other antineoplastics
    • Current market status
    • Classification of pipeline products
      • Angiogenesis inhibitors
        • Angiogenesis as a normal biological process
        • Angiogenesis is known to be aberrant in tumor cell proliferation
        • Angiogenesis inhibitors as viable antitumor agents can target a number of pathways
        • At present, only one angiogenesis inhibitor exists on the market
      • Single-target signal transduction inhibitors
        • A plethora of potential targets exist along the signaling cascade
        • Several signal transduction inhibitors have reached the market, bringing with them their own sets of issues for consideration
      • Multi-targeted inhibitors
        • Multi-targeted inhibitors have certain advantages over single targeted agents
        • Approval of three multi-targeted inhibitors
      • Cell cycle and apoptosis targeted inhibitors
        • Only one cell cycle inhibitor has entered Phase III
        • Cell death can be induced via a number of different pathways
        • To date, only one apoptosis stimulator has reached the market
      • Epigenetic modulators
        • Despite relative immaturity of development in this class of drugs, the potential to enhance current therapies exists
      • Immunomodulatory and immunoconjugated therapeutics
        • Antibody-based technologies are an effective anticancer approach
    • Oncology clinical trial design
      • Patient selection
        • Increasingly significant in the era of targeted treatment
      • Clinical trial duration
        • Sufficient follow-up is necessary to establish true clinical benefit
      • The advent of novel therapies
        • Diversity of targeted therapies will require an evolution in clinical trial design
      • Clinical trial endpoints in oncology
        • Most oncology clinical trials designate multiple endpoints
        • Survival
        • Quality of life
        • Tumor response rates
        • Toxicity
        • Time to tumor progression
  • CHAPTER 4 PIPELINE ANGIOGENESIS INHIBITORS ANALYSIS & FORECASTS
    • Overview of angiogenesis inhibitors
      • Pipeline summary
        • Late-phase pipeline of angiogenesis inhibitors
        • Phase II pipeline of angiogenesis inhibitors
        • Phase I pipeline of angiogenesis inhibitors
      • Comparative forecasts
      • Definition of current comparator therapy
        • Avastin (Bevacizumab; Genentech/Roche/Chugai)
    • Aflibercept (VEGF-Trap; Sanofi Aventis/Regeneron)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Interim Phase II results for aflibercept in ovarian cancer
        • Interim Phase II results for aflibercept in NSCLC
        • Aflibercept demonstrates similar side effects to Avastin
      • Datamonitor comments
        • Fierce competition with Avastin in the wider cancer market
        • Presence in oncology field will aid commercialization of aflibercept
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Pazopanib (GW786034; GlaxoSmithKline)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Pazopanib as a possible second-line monotherapy treatment for metastatic RCC
        • Co-administration with Tykerb may alter the pharmacokinetics of pazopanib - Phase III studies planned
        • Pazopanib showing applicability across a broad range of solid tumor types
      • Datamonitor comments
        • Initial approval in RCC will force pazopanib to compete against the already approved Sutent and Nexavar
        • Extensive parallel development program planned
        • Tykerb may well enhance the success of pazopanib but at what price?
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Recentin (Cediranib, AZD2171; AstraZeneca)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • AstraZeneca targets first-line CRC
        • Recentin has potential in NSCLC in combination with standard chemotherapy regimens
        • Phase III study planned for Recentin in glioma
      • Datamonitor comments
        • As a potentially more potent inhibitor of angiogenesis, and given its formulation, Recentin' s future may be highly promising
        • Phase III studies in CRC are high-risk while development in glioma may offer a quicker route to market
        • AstraZeneca' s strength in the oncology market will be key in Recentin' s success
      • Forecasts to 2016
      • Datamonitor drug assessment summary
  • CHAPTER 5 PIPELINE SINGLE-TARGET SIGNAL TRANSDUCTION INHIBITORS ANALYSIS & FORECASTS
    • Overview of single-target signal transduction inhibitors
      • Pipeline summary
        • Late-phase pipeline of single-target signal transduction inhibitors
        • Phase II pipeline of single-target signal transduction inhibitors
        • Phase I pipeline of single-target signal transduction inhibitors
      • Comparative forecasts
      • Definition of current comparator therapy
        • Gleevec (Imatinib; Novartis)
    • Certican (Everolimus, RAD-001; Novartis)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Certican may be a promising addition to the treatment of neuroendocrine tumors
        • Certican is also showing applicability in some of the more common tumor types
      • Datamonitor comments
        • Approval as an anticancer therapy will enable Certican to achieve a significantly higher level of sales
        • NET a good place to start
        • Novartis is an ideal backer for the drug
        • Certican may face stiff competition from Torisel
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Sarasar (Lonafarnib; Schering-Plough)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Main focus of Sarasar is development in MDS, where greatest antitumor activity is shown
        • Farnesyl transferase inhibitors predominately in hematological disorders
        • Lack of efficacy has led to termination of pivotal Phase III trial in NSCLC
        • Lack of clinical data makes it difficult to judge Sarasar' s potential in breast cancer
        • Benefit shown in advanced head and neck cancer, although no further trials have been announced
        • Mild toxicity in the majority of patients, although grade 3 events do occur
      • Datamonitor comments
        • Sarasar' s chances for approval will be delayed beyond 2007
        • Sarasar racing against Johnson & Johnson' s Zarnestra as the first farnesyl transferase inhibitor to reach the market
        • Presence in oncology market will aid commercialization of Sarasar
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • TheraCIM (Nimotuzumab; YM Bioscience)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Phase III underway for pediatric pontine (brain stem) glioma
        • Phase II pediatric trial demonstrated activity
      • Datamonitor comments
        • Phase III trial results required to verify the efficacy of this agent
        • YM Biosciences look to broaden TheraCIM' s horizons
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Xinlay (Atrasentan; Abbott Laboratories)
      • Drug overview
        • Xinlay' s target receptor plays a key role in cancer cell proliferation
      • Key historical events
      • Clinical trial data
        • FDA do not approve Xinlay for prostate cancer
        • Not the end of the road for Xinlay with new Phase III trial now underway
      • Datamonitor comments
        • Despite its rejection by the FDA, Xinlay' s future may still be promising
        • Abbott' s favorable position in the prostate cancer market will be invaluable
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Zalutumumab (HuMax-EGFR; Genmab)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • With Fast Track status granted, SCCHN offers promise as a lead indication for zalutumumab
      • Datamonitor comments
        • A head-to-head study against Erbitux could work in zalutumumab' s favor
        • Zalutumumab will need to be competitively priced
        • Zalutumumab may also have to compete with Tarceva and Iressa
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Zarnestra (Tipifarnib; Johnson & Johnson)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Following rejection of NDA, the FDA requires Phase III data for Zarnestra in AML before regulatory approval can be considered
        • Results from Phase III studies have yet to be announced
        • Zarnestra has demonstrated a favorable profile in Phase II studies
        • Single-agent Zarnestra demonstrates antitumor activity in relapsed/refractory aggressive NHL
        • Zarnestra holding promise in juvenile myelomonocytic leukemia
        • Following modest activity in brain cancer, further trials have been initiated
        • Negative Phase III trial results cause termination of development in pancreatic and colorectal cancer
      • Datamonitor comments
        • Schering-Plough' s Sarasar catching up with Zarnestra as the first farnesyl transferase inhibitor to reach the market
        • Johnson & Johnson limiting Zarnestra' s target population in the short term
        • Johnson & Johnson' s experience will be invaluable to Zarnestra
      • Forecasts to 2016
      • Datamonitor drug assessment summary
  • CHAPTER 6 PIPELINE MULTI-TARGETED INHIBITORS ANALYSIS & FORECASTS
    • Overview of multi-targeted inhibitors
      • Pipeline summary
        • Late-phase pipeline of multi-targeted inhibitors
        • Phase II pipeline of multi-targeted inhibitors
        • Phase I pipeline of multi-targeted inhibitors
      • Comparative forecasts
      • Definition of current comparator therapy
        • Gleevec (Imatinib; Novartis)
    • Tasigna (Nilotinib, AMN-107; Novartis)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Tasigna awaiting approval in the US, the EU and Japan for Gleevec-resistant CML
        • Promising Phase II data reported
        • Tasigna appears effective in CML patients who have failed or are intolerant to both Gleevec and Sprycel
        • Only one Bcr-Abl mutation is insensitive to Tasigna
        • Tasigna shows promise for Gleevec-resistant metastatic GIST patients
      • Datamonitor comments
        • Tasigna ready to challenge Bristol-Myers Squibb' s already approved Sprycel
        • Novartis looking to expand its leading role in the CML therapy market
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Axitinib (AG-13736; Pfizer)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Phase III trial warranted in pancreatic cancer following a 26% reduction in the risk of death when axitinib is added to Gemzar - Phase II results
        • Axitinib demonstrates impressive activity in thyroid cancer. Phase III trial yet to start
        • Axitinib also making encouraging progress in other popular tumor types
      • Datamonitor comments
        • A similar response rate to Tarceva in pancreatic cancer means approval will be likely
        • Axitinib will enjoy the global presence and unparalleled marketing strength Pfizer can offer
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Ceflatonin (Myelostat; ChemGenex Pharmaceuticals)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Ceflatonin aims to restore Gleevec sensitivity in CML patients
        • ChemGenex looking to expand Ceflatonin into the AML/APL market
      • Datamonitor comments
        • Despite convincing clinical benefit, Ceflatonin will face strong competition from Bristol-Myers Squibb' s Sprycel and Novartis' s Tasigna
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Enzastaurin (LY317615; Eli Lilly)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Enzastaurin looking to make its mark in the B-cell lymphoma market
        • Enzastaurin holding promise as a maintenance therapy in mantle cell lymphoma
        • Despite discontinuation of a Phase III trial in Glioma, Eli Lilly has initiated 20 additional clinical trials
      • Datamonitor comments
        • Eli Lilly adopt a risky strategy for enzastaurin in DLBCL
        • Termination of Phase III trial for enzastaurin in glioma may hamper its potential in other indications
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Lestaurtinib (CEP-701; Cephalon)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Lestaurtinib emerging as a promising agent for AML patients harboring Flt-3 activating mutations
      • Datamonitor comments
        • Lestaurtinib may be the first in its class to reach the market
        • Cephalon' s recent acquisition of Trisenox will provide valuable experience of the leukemia market
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Zactima (Vandetanib, ZD6474; AstraZeneca)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Zactima granted Orphan Drug designation and Fast Track status for Thyroid cancer
        • Multiple Phase III trials for Zactima underway in NSCLC
        • Zactima fails to demonstrate efficacy as a maintenance therapy for SCLC
      • Datamonitor comments
        • Zactima set to enjoy a monopoly of thyroid cancer niche market
        • Zactima being pushed through the clinical development process for NSCLC
        • Zactima offers product differentiation with unique multi-targeted characteristics
        • AstraZeneca' s strength in the oncology market will be key in Zactima' s success
      • Forecasts to 2016
      • Datamonitor drug assessment summary
  • CHAPTER 7 PIPELINE CELL CYCLE AND APOPTOSIS TARGETED AGENTS ANALYSIS & FORECASTS
    • Overview of cell cycle and apoptosis targeted agents
      • Pipeline summary
        • Late-phase pipeline of cell cycle and apoptosis targeted agents
        • Phase II pipeline of cell cycle and apoptosis targeted agents
        • Phase I pipeline of cell cycle and apoptosis targeted agents
      • Comparative forecasts
      • Definition of current comparator therapy
        • Velcade (Bortezomib; Millennium Pharmaceuticals)
    • Alvocidib (Flavopiridol; Sanofi-Aventis)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Continuous infusion dosing schedules fail to demonstrate clinical activity
        • Modified dosing regimen drives further development in CLL
      • Datamonitor comments
        • Given alvocidib' s checkered history, Sanofi-Aventis may face an uphill struggle communicating the drug' s potential
        • Alvocidib may show more promise as part of a combination regimen
        • Presence in oncology field will aid commercialization of alvocidib
    • Genasense (Oblimersen; Genta)
      • Drug overview
      • Key historical events
      • Datamonitor comments
        • Approval of Genasense is looking increasingly unlikely
        • Termination of agreement with Sanofi-Aventis is a major setback for Genta
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Phenoxodiol (Novogen)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • The OVATURE trials
        • The combination of phenoxodiol and cisplatin is particularly effective in ovarian cancer
      • Datamonitor comments
        • Toxicity will be the key factor for phenoxodiol' s success
        • Sanofi-Aventis as a marketing partner?
      • Forecasts to 2016
      • Datamonitor drug assessment summary
  • CHAPTER 8 PIPELINE IMMUNOMODULATORY AND IMMUNOCONJUGATED THERAPEUTICS ANALYSIS & FORECASTS
    • Overview of immunomodulatory and immunoconjugated therapeutics
      • Pipeline summary
        • Late-phase pipeline of immunomodulatory and immunoconjugated therapeutics
        • Phase II pipeline of immunomodulatory and immunoconjugated therapeutics
        • Phase I pipeline of immunomodulatory and immunoconjugated therapeutics
      • Comparative forecasts
      • Definition of current comparator therapy
        • Rituxan (Rituximab; Biogen Idec/Genentech/Roche)
    • Galiximab (Anti-CD80 MAb; Biogen Idec)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Randomized Phase III trial will compare survival of galiximab plus Rituxan with Rituxan alone in relapsed/refractory follicular NHL patients
        • Phase II results show galiximab and Rituxan can be safely combined and can produce promising response rates in follicular NHL patients
      • Datamonitor comments
        • Biogen Idec in a strong position to successfully market galiximab alone
        • Biogen-Idec will need to effectively demonstrate the value of a combination of galiximab and Rituxan to payers
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Lumiliximab (Anti-CD23 MAb; Biogen Idec)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • The addition of lumiliximab to the FCR regimen may produce a higher response rate without additional toxicity
      • Datamonitor comments
        • Lumiliximab on course to become an established addition to the standard treatment for CLL
        • Biogen Idec should look to investigate Lumiliximab as a maintenance therapy
        • Cluster of Differentiation (CD) drugs have become Biogen Idec' s specialty
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Ofatumumab (HuMax-CD20; Genmab/GlaxoSmithKline)
      • Drug overview
        • Genmab hoping ofatumumab will demonstrate a preferred efficacy profile over Rituxan in the clinic
      • Key historical events
      • Clinical trial data
        • Ofatumumab receives Fast Track status for CLL and enters a Phase III trial
        • Genmab initiates a pivotal Phase III trial in follicular NHL
      • Datamonitor comments
        • Ofatumumab may offer hope for Rituxan-insensitive patients
        • Approval of other MAbs being developed by Biogen Idec for NHL and CLL may restrict ofatumumab' s potential even further
        • GlaxoSmithKline will offer invaluable experience to Genmab and aid commercialization of ofatumumab
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Proxinium/Vicinium (VB4-845; Viventia Biotech)
      • Drug overview
        • An ' armed' antibody for the potential treatment of head and neck, and bladder cancer
      • Key historical events
      • Clinical trial data
        • Proxinium shows a good safety profile and preliminary evidence of clinical efficacy in Phase I trials in head and neck cancer
        • Vicinium also making headway in bladder cancer
      • Datamonitor comments
        • The requirement for EpCAM expression may limit Proxinium' s uptake
        • Proxinium will have to compete with Erbitux
        • Viventia should look to investigate Proxinium in combination with radiotherapy
        • BCG failure creates a commercial opportunity for Vicinium
        • Vicinium may face competitive pressure from novel intravesical chemotherapies in the near future
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Rencarex (WX-G250; Wilex)
      • Drug overview
        • MN/CA IX Antigen - A highly specific tumor target
        • Mode of Action of Rencarex - ADCC
      • Key historical events
      • Clinical trial data
        • Completed Phase I & II trials for metastatic RCC
        • In patients responding to treatment, Rencarex monotherapy improves survival
        • The combination with IFN is well-tolerated and of clinical benefit in metastatic RCC
      • Datamonitor comments
        • The high recurrence rate for RCC creates a commercial opportunity
        • Rencarex may face a number of hurdles
      • Forecasts to 2016
      • Datamonitor drug assessment summary
    • Zanolimumab (HuMax-CD4; Genmab)
      • Drug overview
      • Key historical events
      • Clinical trial data
        • Zanolimumab' s Orphan Drug and Fast Track status reflects the high unmet needs in CTCL
        • Zanolimumab may also hold promise for PTCL patients
      • Datamonitor comments
        • The T-cell lymphoma market offers zanolimumab a limited commercial potential
        • Depletion of CD4+ T-cells by zanolimumab may render the patient susceptible to opportunistic infections
      • Forecasts to 2016
      • Datamonitor drug assessment summary
  • CHAPTER 9 PIPELINE EPIGENETIC MODULATORS ANALYSIS & FORECASTS
    • Overview of epigenetic modulators
      • Pipeline summary
        • Late-phase pipeline of epigenetic modulators
        • Phase II pipeline of epigenetic modulators
        • Phase I pipeline of epigenetic modulators
  • APPENDIX
    • List of tables
    • List of figures
    • Methodology
      • Datamonitor forecast methodology
        • Epidemiology forecasts
        • Product forecasts
      • Datamonitor drug assessment summary
    • Abbreviations
    • Contributing experts
    • Bibliography
    • About Datamonitor
      • About Datamonitor Healthcare
    • Datamonitor Healthcare' s therapy area capabilities
      • About the Disease analysis team
      • Disclaimer
    • List of Tables
      • Table 1: Late-phase pipeline molecular targeted cancer therapies, 2007
      • Table 2: Phase II pipeline molecular targeted cancer therapies, 2007
      • Table 3: Phase I pipeline molecular targeted cancer therapies, 2007
      • Table 4: Pipeline molecular targeted therapies by development phase and class of drug, 2007
      • Table 5: Pipeline molecular targeted therapies by indication, 2007
      • Table 6: Potential anticancer molecular targets being exploited by only one candidate in the clinical development pipeline, 2007
      • Table 7: Potential anticancer molecular targets being exploited by two candidates in the clinical development pipeline, 2007
      • Table 8: Potential anticancer molecular targets being exploited by three candidates in the clinical development pipeline, 2007
      • Table 9: Pfizer' s marketed cancer portfolio, 2007
      • Table 10: Pfizer' s molecular targeted cancer therapies pipeline, 2007
      • Table 11: AstraZeneca' s marketed cancer portfolio, 2007
      • Table 12: AstraZeneca' s molecular targeted cancer therapies pipeline, 2007
      • Table 13: Novartis' s marketed cancer portfolio, 2007
      • Table 14: Novartis' s molecular targeted cancer therapies pipeline, 2007
      • Table 15: Late-phase pipeline molecular targeted therapy products sales forecasts in the seven major markets ($m), 2007-2016
      • Table 16: Currently approved molecular targeted cancer therapies, 2007
      • Table 17: Examples of naturally occurring angiogenesis stimulators
      • Table 18: Recently approved multi-targeted inhibitors, 2007
      • Table 19: Late-phase pipeline angiogenesis inhibitors, 2007
      • Table 20: Phase II pipeline angiogenesis inhibitors, 2007
      • Table 21: Phase I pipeline angiogenesis inhibitors, 2007
      • Table 22: Forecasting assumptions for late-phase angiogenesis inhibitors in the seven major pharmaceutical markets, 2007 (1 of 2)
      • Table 23: Forecasting assumptions for late-phase angiogenesis inhibitors in the seven major pharmaceutical markets, 2007 (2 of 2)
      • Table 24: Avastin: Key facts
      • Table 25: Aflibercept: Key historical events
      • Table 26: Ongoing clinical trials involving aflibercept, 2007
      • Table 27: Interim Phase II results for aflibercept in NSCLC
      • Table 28: Forecasting assumptions for aflibercept in the seven major pharmaceutical markets, 2007
      • Table 29: Aflibercept 7MM sales forecast in second-line ovarian cancer, second-line NSCLC and second-line HRPC ($m), 2007-2016
      • Table 30: Pazopanib: Key historical events
      • Table 31: Ongoing clinical trials involving pazopanib, 2007
      • Table 32: Phase II interim analysis for pazopanib monotherapy in second-line RCC at 12 weeks
      • Table 33: Phase II interim analysis for pazopanib monotherapy in relapsed soft tissue sarcoma at 12 weeks
      • Table 34: Phase II interim analysis for pazopanib monotherapy in high-risk relapsed ovarian cancer at 12 weeks
      • Table 35: Forecasting assumptions for pazopanib in the seven major pharmaceutical markets, 2007
      • Table 36: Pazopanib 7MM sales forecast in first/second-line RCC and second-line Her2+ breast cancer ($m), 2007-2016
      • Table 37: Recentin: Key historical events
      • Table 38: Ongoing clinical trials involving Recentin, 2007
      • Table 39: Phase I results of Recentin plus standard chemotherapy in NSCLC
      • Table 40: Forecasting assumptions for Recentin in the seven major pharmaceutical markets, 2007
      • Table 41: Recentin 7MM sales forecast in first-line NSCLC, first-line CRC and recurrent/ progressive glioma ($m), 2007-2016
      • Table 42: Late-phase pipeline single-target signal transduction inhibitors, 2007
      • Table 43: Phase II pipeline single-target signal transduction inhibitors, 2007
      • Table 44: Phase I pipeline single-target signal transduction inhibitors, 2007
      • Table 45: Forecasting assumptions for late-phase single-target signal transduction inhibitors in the seven major pharmaceutical markets, 2007 (1 of 3)
      • Table 46: Forecasting assumptions for late-phase single-target signal transduction inhibitors in the seven major pharmaceutical markets, 2007 (2 of 3)
      • Table 47: Forecasting assumptions for late-phase single-target signal transduction inhibitors in the seven major pharmaceutical markets, 2007 (3 of 3)
      • Table 48: Gleevec: Key facts
      • Table 49: Certican: Key historical events
      • Table 50: Ongoing clinical trials involving Certican, 2007
      • Table 51: Phase II study results for Certican plus octreotide in NET
      • Table 52: Interim Phase II results of Certican monotherapy in metastatic RCC
      • Table 53: Interim Phase II results of Certican monotherapy in lymphoma
      • Table 54: Forecasting assumptions for Certican in the seven major pharmaceutical markets, 2007
      • Table 55: Certican 7MM sales forecast in second-line NET, second-line RCC, salvage therapy CRC and second-line GIST ($m), 2007-2016
      • Table 56: Sarasar: Key historical events
      • Table 57: Ongoing clinical trials involving Sarasar, 2007
      • Table 58: Phase I/II study results of Sarasar monotherapy in advanced MDS and CMML (1 of 2)
      • Table 59: Phase I/II study results of Sarasar monotherapy in advanced MDS and CMML (2 of 2)
      • Table 60: Phase II results of Sarasar in Head and Neck cancer
      • Table 61: Forecasting assumptions for Sarasar in the seven major pharmaceutical markets, 2007
      • Table 62: Sarasar 7MM sales forecast in second-line MDS ($m), 2007-2016
      • Table 63: TheraCIM: Key historical events
      • Table 64: Ongoing clinical trials involving TheraCIM, 2007
      • Table 65: Forecasting assumptions for TheraCIM in the seven major pharmaceutical markets, 2007
      • Table 66: TheraCIM 7MM sales forecast in first-line glioma ($m), 2007-2016
      • Table 67: Xinlay: Key historical events
      • Table 68: Ongoing clinical trials involving Xinlay, 2007
      • Table 69: Meta-analysis of pooled data from two randomized Phase III trials (M96-594 and M00-211) of Xinlay versus placebo in metastatic HRPC
      • Table 70: Forecasting assumptions for Xinlay in the seven major pharmaceutical markets, 2007
      • Table 71: Xinlay 7MM sales forecast in first-line metastatic HRPC ($m), 2007-2016
      • Table 72: Zalutumumab: Key historical events
      • Table 73: Ongoing clinical trials involving zalutumumab, 2007
      • Table 74: Phase I/II study results of zalutumumab in recurrent SCCHN
      • Table 75: Forecasting assumptions for zalutumumab in the seven major pharmaceutical markets, 2007
      • Table 76: Zalutumumab 7MM sales forecast in first/second-line SCCHN ($m), 2007-2016
      • Table 77: Zarnestra: Key historical events
      • Table 78: Ongoing clinical trials involving Zarnestra, 2007
      • Table 79: Phase I/II study of Zarnestra in combination with chemotherapy in newly diagnosed AML or high-risk MDS patients
      • Table 80: Phase II results for Zarnestra in elderly, previously untreated poor-risk AML patients who were not suitable for chemotherapy
      • Table 81: Phase II results of Zarnestra monotherapy in relapsed/refractory aggressive NHL, 2006
      • Table 82: Phase II study results of Zarnestra in juvenile myelomonocytic leukemia (JMML), 2005
      • Table 83: Phase I/II trial involving Nexavar, Tarceva, Torisel and Zarnestra, 2006
      • Table 84: Phase III trial results of Zarnestra in pancreatic cancer
      • Table 85: Phase III trial results of Zarnestra in CRC
      • Table 86: Forecasting assumptions for Zarnestra in the seven major pharmaceutical markets, 2007
      • Table 87: Zarnestra 7MM sales forecasts in first-line elderly AML ($m), 2007-2016
      • Table 88: Late-phase pipeline multi-targeted inhibitors, 2007
      • Table 89: Phase II pipeline multi-targeted inhibitors, 2007
      • Table 90: Phase I pipeline multi-targeted inhibitors, 2007
      • Table 91: Forecasting assumptions for late-phase multi-targeted inhibitors in the seven major pharmaceutical markets, 2007 (1 of 2)
      • Table 92: Forecasting assumptions for late-phase multi-targeted inhibitors in the seven major pharmaceutical markets, 2007 (2 of 2)
      • Table 93: Gleevec: Key facts
      • Table 94: Tasigna: Key historical events
      • Table 95: Ongoing clinical trials involving Tasigna, 2007
      • Table 96: Trial design and clinical outcomes for a small patient subgroup from the ENACT trial
      • Table 97: Phase II results for Tasigna in Gleevec-resistant or intolerant patients with CML in chronic phase
      • Table 98: Phase II results for Tasigna in Gleevec-resistant or intolerant patients with CML in accelerated phase
      • Table 99: Phase II results for Tasigna in Gleevec-resistant or intolerant patients with CML in blast crisis phase or relapsed/refractory Ph+ ALL
      • Table 100: Phase II results for Tasigna in hypereosinophilic syndrome (HES)
      • Table 101: Phase II results for Tasigna in systemic mastocytosis
      • Table 102: Phase II results for Tasigna in Gleevec and Sprycel-resistant or intolerant patients with CML in all stages of the disease
      • Table 103: Phase I results for Tasigna with or without Gleevec in Gleevec-resistant GIST
      • Table 104: Forecasting assumptions for Tasigna in the seven major pharmaceutical markets, 2007
      • Table 105: Tasigna sales forecast in Gleevec-refractory CML and third-line GIST ($m), 2007-2016
      • Table 106: Axitinib: Key historical events
      • Table 107: Ongoing clinical trials involving axitinib, 2007
      • Table 108: Phase II results for axitinib in thyroid cancer
      • Table 109: Phase II results for axitinib in Nexavar-refractory mRCC
      • Table 110: Phase II results for axitinib in relapsed NSCLC
      • Table 111: Forecasting assumptions for axitinib in the seven major pharmaceutical markets, 2007
      • Table 112: Axitinib 7MM sales forecast in first-line pancreatic cancer and second-line thyroid cancer ($m), 2007-2016
      • Table 113: Ceflatonin: Key historical events
      • Table 114: Ongoing clinical trials involving Ceflatonin, 2007
      • Table 115: Interim data for Ceflatonin monotherapy in patients with Gleevec-refractory CML harboring the T315I Bcr-Abl point mutation
      • Table 116: Phase II trial outline for Ceflatonin plus Gleevec in Gleevec-refractory patients
      • Table 117: Interim data for Ceflatonin in combination with Gleevec in patients with Gleevec-refractory CML
      • Table 118: Forecasting assumptions for Ceflatonin in the seven major pharmaceutical markets, 2007
      • Table 119: Ceflatonin 7MM sales forecast in Gleevec-resistant CML ($m), 2007-2016
      • Table 120: Enzastaurin: Key historical events
      • Table 121: Ongoing clinical trials involving enzastaurin, 2007
      • Table 122: Phase II results of enzastaurin in relapsed DLBCL
      • Table 123: Phase II results of enzastaurin in relapsed MCL
      • Table 124: Phase II results of enzastaurin in second/third-line NSCLC
      • Table 125: Forecasting assumptions for enzastaurin in the seven major pharmaceutical markets, 2007
      • Table 126: Enzastaurin 7MM sales forecast as a maintenance therapy in DLBCL ($m), 2007-2016
      • Table 127: Lestaurtinib: Key historical events
      • Table 128: Ongoing clinical trial involving lestaurtinib, 2007
      • Table 129: Interim Phase II/III results of lestaurtinib and chemotherapy in patients with relapsed AML harboring Flt-3 activating mutations
      • Table 130: Forecasting assumptions for lestaurtinib in the seven major pharmaceutical markets, 2007
      • Table 131: Lestaurtinib 7MM sales forecast in second-line AML ($m), 2007-2016
      • Table 132: Zactima' s multiple anticancer targets
      • Table 133: Zactima: Key historical events
      • Table 134: Ongoing clinical trials involving Zactima, 2007
      • Table 135: Phase II results for Zactima monotherapy in metastatic hereditary medullary thyroid cancer
      • Table 136: Phase II results for Zactima plus chemotherapy in first-line NSCLC
      • Table 137: Phase II results for Zactima plus Taxotere in second-line NSCLC
      • Table 138: Phase I results for Zactima plus Alimta in second-line NSCLC
      • Table 139: Forecasting assumptions for Zactima in the seven major pharmaceutical markets, 2007
      • Table 140: Zactima 7MM sales forecast in NSCLC ($m), 2007-2016
      • Table 141: Late-phase pipeline cell cycle and apoptosis targeted agents, 2007
      • Table 142: Phase II pipeline cell cycle and apoptosis targeted agents, 2007
      • Table 143: Phase I pipeline cell cycle and apoptosis targeted agents, 2007
      • Table 144: Forecasting assumptions for late-phase cell cycle and apoptosis targeted agents in the seven major pharmaceutical markets, 2007
      • Table 145: Velcade: Key facts
      • Table 146: Alvocidib: Key historical events
      • Table 147: Ongoing clinical trials involving alvocidib, 2007
      • Table 148: Genasense: Key historical events
      • Table 149: Forecasting assumptions for Genasense in the seven major pharmaceutical markets, 2007
      • Table 150: Genasense 7MM sales forecast in first-line elderly AML and first-line metastatic melanoma ($m), 2007-2016
      • Table 151: Phenoxodiol: Key historical events
      • Table 152: Ongoing clinical trials involving phenoxodiol, 2007
      • Table 153: Forecasting assumptions for phenoxodiol in the seven major pharmaceutical markets, 2007
      • Table 154: Phenoxodiol 7MM sales forecast in third-line ovarian cancer ($m), 2007-2016
      • Table 155: Late-phase pipeline immunomodulatory and immunoconjugated therapeutics, 2007
      • Table 156: Phase II pipeline immunomodulatory and immunoconjugated therapeutics, 2007
      • Table 157: Phase I pipeline immunomodulatory and immunoconjugated therapeutics, 2007
      • Table 158: Forecasting assumptions for late-phase immunomodulatory and immunoconjugated therapeutics in the seven major pharmaceutical markets, 2007 (1 of 2)
      • Table 159: Forecasting assumptions for late-phase immunomodulatory and immunoconjugated therapeutics in the seven major pharmaceutical markets, 2007 (2 of 2)
      • Table 160: Approved indications for Rituxan in the US and EU, 2006
      • Table 161: Rituxan: Key facts
      • Table 162: Galiximab: Key historical events
      • Table 163: Ongoing clinical trial involving galiximab, 2007
      • Table 164: Phase II study of galiximab in combination with Rituxan in relapsed/refractory follicular NHL
      • Table 165: Retrospective comparison of galiximab plus Rituxan with Rituxan monotherapy in relapsed/refractory follicular NHL
      • Table 166: Forecasting assumptions for galiximab in the seven major pharmaceutical markets, 2007
      • Table 167: Galiximab 7MM sales forecast in follicular NHL ($m), 2007-2016
      • Table 168: Lumiliximab: Key historical events
      • Table 169: Ongoing clinical trial involving lumiliximab, 2007
      • Table 170: Comparison of results from a Phase I/II study of lumiliximab in combination with FCR in relapsed/refractory CLL
      • Table 171: Biogen Idec' s Cluster of Differentiation (CD) targeted drugs, 2007
      • Table 172: Forecasting assumptions for lumiliximab in the seven major pharmaceutical markets, 2007
      • Table 173: Lumiliximab 7MM sales forecast in relapsed/refractory CLL ($m), 2007-2016
      • Table 174: Ofatumumab: Key historical events
      • Table 175: Ongoing clinical trial involving ofatumumab, 2007
      • Table 176: Phase I/II results of ofatumumab in relapsed/refractory CLL
      • Table 177: Interim Phase I/II results of ofatumumab in relapsed/refractory follicular NHL
      • Table 178: Phase I/II adverse events data from ofatumumab in relapsed/refractory follicular NHL
      • Table 179: GlaxoSmithKline' s marketed oncology portfolio, 2007
      • Table 180: Forecasting assumptions for ofatumumab in the seven major pharmaceutical markets, 2007
      • Table 181: Ofatumumab 7MM sales forecast in relapsed/refractory CLL and second-line follicular NHL ($m), 2007-2016
      • Table 182: Proxinium: Key historical events
      • Table 183: Ongoing clinical trials involving Proxinium, 2007
      • Table 184: Forecasting assumptions for Proxinium in the seven major pharmaceutical markets, 2007
      • Table 185: Proxinium 7MM sales forecast in second-line SCCHN ($m), 2007-2016
      • Table 186: Rencarex: Key historical events
      • Table 187: Ongoing clinical trials involving Rencarex, 2007
      • Table 188: Phase I/II study of Rencarex plus IFN in metastatic RCC
      • Table 189: Ongoing Phase III trials in the adjuvant RCC setting
      • Table 190: Forecasting assumptions for Rencarex in the seven major pharmaceutical markets, 2007
      • Table 191: Rencarex 7MM sales forecast in adjuvant RCC ($m), 2007-2016
      • Table 192: Zanolimumab: Key historical events
      • Table 193: Ongoing clinical trial involving zanolimumab, 2007
      • Table 194: Phase II results of zanolimumab in mycosis fungoides CTCL
      • Table 195: Interim Phase II results of zanolimumab in PTCL patients
      • Table 196: Forecasting assumptions for zanolimumab in the seven major pharmaceutical markets, 2007
      • Table 197: Zanolimumab 7MM sales forecast in relapsed CTCL ($m), 2007-2016
      • Table 198: Zolinza: Key facts
      • Table 199: Phase II pipeline epigenetic modulators, 2007
      • Table 200: Phase I pipeline epigenetic modulators, 2007
      • Table 201: Datamonitor drug assessment parameters
      • Table 202: Abbreviations used in Pipeline Insight: Molecular Targeted Cancer Therapies
    • List of Figures
      • Figure 1: Pipeline molecular targeted therapies by development phase and class of drug, 2007
      • Figure 2: Pipeline molecular targeted therapies by class of drug, 2007
      • Figure 3: Pipeline molecular targeted therapies by development phase, 2007
      • Figure 4: Angiogenesis inhibitors by developmental phase, 2007
      • Figure 5: Single-target signal transduction inhibitors by developmental phase, 2007
      • Figure 6: Multi-targeted inhibitors by developmental phase, 2007
      • Figure 7: Cell cycle and apoptosis targeted agents by developmental phase, 2007
      • Figure 8: Immunomodulatory and immunoconjugated therapeutics by developmental phase, 2007
      • Figure 9: Epigenetic modulators by developmental phase, 2007
      • Figure 10: Pipeline molecular targeted therapies by indication, 2007
      • Figure 11: Pipeline molecular targeted therapies by hematological malignancy, 2007
      • Figure 12: Potential anticancer molecular targets being exploited by four or more candidates in the clinical development pipeline, 2007
      • Figure 13: Molecular targeted therapies product pipeline by type of company, 2007
      • Figure 14: Segmentation of companies according to number of products in the MTT pipeline, 2007
      • Figure 15: Companies with MTT candidates in late-phase development, 2007
      • Figure 16: Companies with four or more candidates in the molecular targeted therapies pipeline, 2007
      • Figure 17: Pipeline angiogenesis inhibitors sales forecasts across the seven major markets ($m), 2007-2016
      • Figure 18: Pipeline single-target signal transduction inhibitors sales forecasts across the seven major markets ($m), 2007-2016
      • Figure 19: Pipeline multi-targeted inhibitors sales forecasts across the seven major markets ($m), 2007-2016
      • Figure 20: Pipeline cell cycle and apoptosis targeted agents sales forecasts across the seven major markets ($m), 2007-2016
      • Figure 21: Pipeline immunomodulatory and immunoconjugated therapeutics sales forecasts across the seven major markets ($m), 2007-2016
      • Figure 22: Clinical and commercial attractiveness of pipeline angiogenesis inhibitors, 2007
      • Figure 23: Clinical and commercial attractiveness of pipeline single-target signal transduction inhibitors, 2007
      • Figure 24: Clinical and commercial attractiveness of pipeline multi-targeted inhibitors, 2007
      • Figure 25: Clinical and commercial attractiveness of pipeline cell cycle and apoptosis targeted agents, 2007
      • Figure 26: Clinical and commercial attractiveness of pipeline immunomodulatory and immunoconjugated therapeutics, 2007
      • Figure 27: The process of tumor angiogenesis
      • Figure 28: Clinical and commercial attractiveness of pipeline angiogenesis inhibitors, 2007
      • Figure 29: Pipeline angiogenesis inhibitors sales forecasts in the seven major markets ($m), 2007-2016
      • Figure 30: Interim Phase II results of aflibercept in ovarian cancer
      • Figure 31: Aflibercept 7MM sales forecast in second-line ovarian cancer, second-line NSCLC and second-line HRPC ($m), 2007-2016
      • Figure 32: Clinical and commercial attractiveness of aflibercept, 2007
      • Figure 33: Pazopanib' s mode of action
      • Figure 34: Phase III study design for pazopanib monotherapy in second-line RCC
      • Figure 35: Phase II study design for pazopanib monotherapy in second-line RCC
      • Figure 36: Phase II study design for pazopanib monotherapy in relapsed soft tissue sarcoma
      • Figure 37: Phase II study design for pazopanib monotherapy in high-risk relapsed ovarian cancer
      • Figure 38: Pazopanib 7MM sales forecast in first/second-line RCC and second-line Her2+ breast cancer ($m), 2007-2016
      • Figure 39: Clinical and commercial attractiveness of pazopanib, 2007
      • Figure 40: Recentin (cediranib; AZD2171) mode of action
      • Figure 41: Phase I interim results for Recentin in second-line CRC
      • Figure 42: HORIZON II and HORIZON III clinical trials designs involving Recentin in first-line CRC
      • Figure 43: Recentin 7MM sales forecast in first-line NSCLC, first-line CRC and recurrent/ progressive glioma ($m), 2007-2016
      • Figure 44: Clinical and commercial attractiveness of Recentin, 2007
      • Figure 45: Clinical and commercial attractiveness of pipeline single-target signal transduction inhibitors, 2007
      • Figure 46: Pipeline single-target signal transduction inhibitors sales forecasts in the seven major markets ($m), 2007-2016
      • Figure 47: Phase II results of Certican monotherapy in breast cancer
      • Figure 48: Phase II results of Certican monotherapy in NSCLC
      • Figure 49: Certican 7MM sales forecast in second-line NET, second-line RCC, salvage therapy CRC and second-line GIST ($m), 2007-2016
      • Figure 50: Clinical and commercial attractiveness of Certican, 2007
      • Figure 51: Sarasar 7MM sales forecast in second-line MDS ($m), 2007-2016
      • Figure 52: Clinical and commercial attractiveness of Sarasar, 2007
      • Figure 53: Phase II trial results for TheraCIM in pediatric glioma
      • Figure 54: TheraCIM 7MM sales forecast in first-line glioma ($m), 2007-2016
      • Figure 55: Clinical and commercial attractiveness of TheraCIM, 2007
      • Figure 56: Clinical trial design for the recently initiated Phase III trial involving Xinlay in HRPC
      • Figure 57: Xinlay 7MM sales forecast in first-line metastatic HRPC ($m), 2007-2016
      • Figure 58: Clinical and commercial attractiveness of Xinlay, 2007
      • Figure 59: Types of monoclonal antibodies
      • Figure 60: Zalutumumab 7MM sales forecast in first/second-line SCCHN ($m), 2007-2016
      • Figure 61: Clinical and commercial attractiveness of zalutumumab, 2007
      • Figure 62: Phase I/II trial design of Zarnestra in combination with chemotherapy in newly diagnosed AML or high-risk MDS patients
      • Figure 63: Zarnestra 7MM sales forecasts in first-line elderly AML ($m), 2007-2016
      • Figure 64: Clinical and commercial attractiveness of Zarnestra, 2007
      • Figure 65: Clinical and commercial attractiveness of pipeline multi-targeted inhibitors, 2007
      • Figure 66: Pipeline multi-targeted inhibitors sales forecasts ($m), 2007-2016
      • Figure 67: Phase I study outline for Tasigna with or without Gleevec in Gleevec-resistant GIST
      • Figure 68: Tasigna sales forecast in Gleevec-refractory CML and third-line GIST ($m), 2007-2016
      • Figure 69: Clinical and commercial attractiveness of Tasigna, 2007
      • Figure 70: Phase II results for axitinib plus Gemzar in first-line pancreatic cancer
      • Figure 71: Randomized Phase II study results for axitinib plus Taxotere in first-line metastatic breast cancer
      • Figure 72: Axitinib 7MM sales forecast in first-line pancreatic cancer and second-line thyroid cancer ($m), 2007-2016
      • Figure 73: Clinical and commercial attractiveness of axitinib, 2007
      • Figure 74: Phase II/III trial for Ceflatonin in Gleevec-refractory CML
      • Figure 75: Ceflatonin 7MM sales forecast in Gleevec-resistant CML ($m), 2007-2016
      • Figure 76: Clinical and commercial attractiveness of Ceflatonin, 2007
      • Figure 77: Enzastaurin 7MM sales forecast as a maintenance therapy in DLBCL ($m), 2007-2016
      • Figure 78: Clinical and commercial attractiveness of enzastaurin, 2007
      • Figure 79: Lestaurtinib 7MM sales forecast in second-line AML ($m), 2007-2016
      • Figure 80: Clinical and commercial attractiveness of lestaurtinib, 2007
      • Figure 81: Phase II results for maintenance Zactima in SCLC
      • Figure 82: Zactima 7MM sales forecast in NSCLC ($m), 2007-2016
      • Figure 83: Clinical and commercial attractiveness of Zactima, 2007
      • Figure 84: Clinical and commercial attractiveness of pipeline cell cycle and apoptosis targeted agents, 2007
      • Figure 85: Pipeline cell cycle and apoptosis targeted agents sales forecasts ($m), 2007-2016
      • Figure 86: Phase I results for alvocidib monotherapy in CLL
      • Figure 87: Phase II results for alvocidib plus chemotherapy in acute leukemias
      • Figure 88: Genasense 7MM sales forecast in first-line elderly AML and first-line metastatic melanoma ($m), 2007-2016
      • Figure 89: Clinical and commercial attractiveness of Genasense, 2007
      • Figure 90: Phase II results for phenoxodiol plus chemotherapy in resistant/refractory ovarian cancer
      • Figure 91: Phenoxodiol 7MM sales forecast in third-line ovarian cancer ($m), 2007-2016
      • Figure 92: Clinical and commercial attractiveness of phenoxodiol, 2007
      • Figure 93: Clinical and commercial attractiveness of pipeline immunomodulatory and immunoconjugated therapeutics, 2007
      • Figure 94: Pipeline immunomodulatory and immunoconjugated therapeutics sales forecasts ($m), 2007-2016
      • Figure 95: Galiximab 7MM sales forecast in follicular NHL ($m), 2007-2016
      • Figure 96: Clinical and commercial attractiveness of galiximab, 2007
      • Figure 97: Phase I/II study design for lumiliximab in combination with FCR in relapsed/refractory CLL
      • Figure 98: Lumiliximab 7MM sales forecast in relapsed/refractory CLL ($m), 2007-2016
      • Figure 99: Clinical and commercial attractiveness of lumiliximab, 2007
      • Figure 100: Phase III study design for ofatumumab in patients with CLL refractory to both fludarabine and Campath
      • Figure 101: Phase III study design for ofatumumab in Rituxan-refractory follicular NHL
      • Figure 102: Ofatumumab 7MM sales forecast in relapsed/refractory CLL and second-line follicular NHL ($m), 2007-2016
      • Figure 103: Clinical and commercial attractiveness of ofatumumab, 2007
      • Figure 104: Phase I results for Proxinium in advanced SCCHN
      • Figure 105: Phase I/II results for Vicinium in superficial TCC of the bladder
      • Figure 106: Proxinium 7MM sales forecast in second-line SCCHN ($m), 2007-2016
      • Figure 107: Clinical and commercial attractiveness of Proxinium, 2007
      • Figure 108: Rencarex induced ADCC
      • Figure 109: Phase II study design for Rencarex monotherapy in advanced RCC
      • Figure 110: Rencarex Phase II results: median survival
      • Figure 111: Phase I/II study design for Rencarex plus IFN in metastatic RCC
      • Figure 112: Rencarex 7MM sales forecast in adjuvant RCC ($m), 2007-2016
      • Figure 113: Clinical and commercial attractiveness of Rencarex, 2007
      • Figure 114: Phase III study design for zanolimumab in CTCL
      • Figure 115: Preliminary results for the first stage of the Phase III study for zanolimumab in CTCL
      • Figure 116: Zanolimumab 7MM sales forecast in relapsed CTCL ($m), 2007-2016
      • Figure 117: Clinical and commercial attractiveness of zanolimumab, 2007
      • Figure 118: Datamonitor drug assessment summary of pipeline molecular targeted therapies in development for hematological malignancies, 2007
Description

[Report]
Pipeline Insight: Molecular Targeted Cancer Therapies - Can anything else revolutionize the market?
Published: 2007/10
Published by : Datamonitor Datamonitor

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