OncoMatch

OncoMatch/Clinical Trials/NCT06060613

Safety and Efficacy of OBX-115 in Advanced Solid Tumors

Is NCT06060613 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies OBX-115 for tumor skin.

Phase 1/2RecruitingObsidian Therapeutics, Inc.NCT06060613Data as of May 2026

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

Check if I qualify

Extracted eligibility criteria

Cancer type

Melanoma

Non-Small Cell Lung Carcinoma

Small Cell Lung Cancer

Biomarker criteria

Excluded: GNA11 mutation

Excluded: GNAQ mutation

Allowed: BRAF targetable mutation

Disease stage

Required: Stage IV

Metastatic disease required

advanced/metastatic melanoma or relapsed refractory metastatic non-small cell lung cancer (NSCLC)

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 2 prior lines

Must have received: anti-PD-1 therapy — systemic therapy for 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

Must have received: anti-PD-L1 therapy — systemic therapy for 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

Must have received: ICI-based regimen — systemic therapy for NSCLC

relapsed or are refractory to approved systemic therapies (approved ICI-based regimen for all appropriate participants and/or an approved targeted therapy for known molecular abnormalities if applicable to their disease)

Cannot have received: second line cytotoxic chemotherapy

Exception: if already received cytotoxic chemotherapy in the first line setting

must not have been exposed to any second line cytotoxic chemotherapy if they have already received cytotoxic chemotherapy in the first line setting

Cannot have received: BRAF inhibitor

Exception: Participants must not have disease progression on a BRAF/MEK inhibitor that was given as the most recent line of therapy

Participants must not have disease progression on a BRAF/MEK inhibitor that was given as the most recent line of therapy

Cannot have received: MEK inhibitor

Exception: Participants must not have disease progression on a BRAF/MEK inhibitor that was given as the most recent line of therapy

Participants must not have disease progression on a BRAF/MEK inhibitor that was given as the most recent line of therapy

Lab requirements

Blood counts

protocol specified hematologic parameters for absolute neutrophil count (anc) and platelet count

Kidney function

adequate kidney function as specified in the protocol

Liver function

adequate liver function as specified in the protocol

Cardiac function

adequate cardiac function as specified in the protocol

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • The Angeles Clinic and Research Institute (Melanoma) · Los Angeles, California
  • USC Norris Comprehensive Cancer Center (Melanoma/NSCLC) · Los Angeles, California
  • Stanford Cancer Institute (Melanoma/NSCLC) · Stanford, California
  • Orlando Health Cancer Institute (Melanoma/NSCLC) · Orlando, Florida
  • James Graham Brown Cancer Center (Melanoma/NSCLC) · Louisville, Kentucky

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify