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.
Treatment: OBX-115 — This 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 qualifyExtracted 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
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?
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