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CMD-193

Phase 1

Neoplasms | Small molecule | Oncology |Pfizer, Inc.|Last Updated: Sep 10, 2009

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
UNCONTROLLEDBiomarker
Total Trials1
Total Enrollment54
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT00161642Study Evaluating CMD-193 in Advanced Malignant Solid TumorsPHASE1 COMPLETED 54Nov 1, 2004Jul 1, 2007Sep 10, 20093 United States
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Study Endpoints
Primary Endpoints
Physical examinations
hematology panels
ECG
Secondary Endpoints
Radiographic tumor evaluations
blood sampling for pharmacokinetic assessments
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Study Design & Arms
AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT
Interventions
NameTypeDescription
CMD-193DRUG -
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Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites3

Inclusion Criteria: * Histologically confirmed malignant solid tumor that has progressed following standard therapy, or for which no standard effective treatment is available * Tumor expression of Lewis Y antigen ( \> or = 20% tumor cells positive for Lewis Y by immunohistochemistry assay) * Easter...

Countries:United States
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