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RecruitingPhase 1, Phase 2NCT06060613

Safety and Efficacy of OBX-115 in Advanced Solid Tumors

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Trial Parameters

ConditionTumor Skin
SponsorObsidian Therapeutics, Inc.
Study TypeINTERVENTIONAL
PhasePhase 1, Phase 2
Enrollment208
SexALL
Min Age18 Years
Max AgeN/A
Start Date2023-10-25
Completion2028-06-30
Interventions
OBX-115

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Brief Summary

This is a study to investigate the safety and efficacy of an investigational OBX-115 regimen in adult participants with advanced solid tumors.

Eligibility Criteria

Inclusion Criteria: 1. Participant must be 18 years of age or older at the time of signing the informed consent. 2. Participant has a histologically confirmed diagnosis of advanced/metastatic melanoma or relapsed refractory metastatic non-small cell lung cancer (NSCLC). 3. Cohort and indication specific criteria as follows: 1. Phase 1 and Phase 2 Cohort 1 (enrollment complete): * Participants with unresectable or metastatic melanoma must have experienced documented radiographic disease progression after systemic therapy containing a programmed cell death protein 1 (PD-1)/programmed death ligand 1 (PD-L1) blocking antibody. * Participants with melanoma must not exceed 2 prior lines of systemic therapy. Neoadjuvant/Adjuvant treatment will not be considered a prior line of systemic therapy unless the participant progressed during or within the 12 weeks after the last dose of the adjuvant PD-1/PD-L1 blocking antibody. 2. Phase 1 and Phase 2 Cohort 2 (recruiting): * Participants with non-sm

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