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IPH4502

Phase 1

Advanced or Metastatic Solid Tumors | Small molecule | Oncology |Innate Pharma S.A.|Last Updated: Jan 7, 2026

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
UNCONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment145
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT06781983Safety and Tolerability of IPH4502 in Patients With Advanced Solid TumorsPHASE1 RECRUITING 145Jan 24, 2025Apr 1, 2029Jan 7, 20267 United States, France
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Study Endpoints
Primary Endpoints
Safety and Tolerability
From time of first dose through treatment period, including the follow-up: up to 24 months

To evaluate the incidence of AEs, SAEs, TEAEs, and DLTs.

Secondary Endpoints
Maximum Observed Plasma Concentration (Cmax)
From time of informed consent through treatment period, including the follow-up: up to 24 months
Area Under the Plasma Concentration (AUC)
From time of informed consent through treatment period, including the follow-up: up to 24 months
Incidence of antidrug antibodies (ADA) against IPH4502
From time of informed consent through treatment period, including the follow-up: up to 24 months
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Study Design & Arms
AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
IPH4502 MonotherapyEXPERIMENTAL -
Interventions
NameTypeDescription
IPH4502DRUGPart 1 (dose escalation) and Part 2 (dose optimization)
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Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites7

Main Inclusion Criteria: * Histologically confirmed, unresectable, locally advanced or metastatic solid tumors that are known to express Nectin-4 * Prior systemic treatment for locally advanced or metastatic disease, yet no therapy with demonstrated clinical benefit for the tumor type is available....

Countries:United StatesFrance
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Recent Changes (Last 90 Days)
LOWMay 26, 2026NCT06781983primaryCompletionDate: changed
LOWMay 24, 2026NCT06781983studyFirstPostDate: changed