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ING-1

Phase 1

Adenocarcinoma | Small molecule | Oncology |XOMA Royalty Corporation|Last Updated: Jun 24, 2005

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 Enrollment30
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT00051675Phase I Study of a Monoclonal Antibody for Treatment of Advanced AdenocarcinomasPHASE1 COMPLETED 30Jul 1, 2002Sep 1, 2003Jun 24, 20051 United States
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Study Design & Arms
AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT
Interventions
NameTypeDescription
ING-1(heMAb)DRUG -
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Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria 1. Subject has adenocarcinomas of the ovary, breast, lung, prostate, colon or rectum. 2. Subject has an advanced metastatic adenocarcinoma that is either refractory to standard therapies or for which therapies that may potentially be of major benefit do not exist. 3. Subject has ...

Countries:United States
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