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Mo-Rez

Phase 1

Tumours, Gynecological | Small molecule | Oncology |GSK plc|Last Updated: May 22, 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
RandomizedCONTROLLEDBiomarker
Total Trials1
Total Enrollment305
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT06796907A Study of Mocertatug Rezetecan in Combination With Anti-cancer Therapies for Advanced Solid TumorsPHASE1 RECRUITING 305Mar 4, 2025Oct 10, 2028May 22, 202678 United States, Argentina +21
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Study Endpoints
Primary Endpoints
Part A: Percentage of participants with dose limiting toxicities (DLTs)
Approximately 7 months
Part A: Number of participants with adverse events (AEs), immune-mediated adverse events (imAEs), adverse events of special interest (AESI), serious adverse events (SAEs) by Severity
Up to approximately 22 months
Part A: Number of participants with adverse events (AEs), immune-mediated adverse events (imAEs), adverse events of special interest (AESI), serious adverse events (SAEs) by Frequency
Up to approximately 22 months
Part B: Confirmed Objective Response Rate (ORR)
Up to approximately 37 months

ORR is defined as the percentage of participants with a best overall confirmed (BOR) of Partial Response (PR) or better per Response Evaluation Criteria in Solid Tumors (RECIST 1.1)

Secondary Endpoints
Part A: Confirmed Objective Response Rate (ORR)
Up to approximately 22 months
Parts A and B: Duration of response (DoR)
Up to approximately 37 months
Parts A and B: Progression-free survival (PFS)
Up to approximately 37 months
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Study Design & Arms
AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
Module 1 (Mo-Rez +Dostarlimab) Endometrial CancerEXPERIMENTAL -
Module 2 (Mo-Rez +/-Bevacizumab) Ovarian CancerEXPERIMENTAL -
Interventions
NameTypeDescription
Mo-RezDRUGMo-Rez will be administered intravenously (IV).
DostarlimabDRUGDostarlimab will be administered IV.
BevacizumabDRUGBevacizumab will be administered IV.
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Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites78

Inclusion Criteria: * Participants must be 18 years of age inclusive or older, at the time of signing the informed consent, or the legal age of consent in the jurisdiction in which the study is taking place. * Participant capable of giving signed informed consent including compliance with the requi...

Countries:United StatesArgentinaAustraliaBelgiumBrazilCanadaDenmarkFinlandFranceGermanyGreeceItalyJapanMexicoNetherlandsNorwayPanamaPolandSouth KoreaSpainSwedenTurkey (Türkiye)United Kingdom
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Recent Changes (Last 90 Days)
HIGHMay 26, 2026NCT06796907Enrollment: 392 → 305
LOWMay 24, 2026NCT06796907studyFirstPostDate: changed