OncoMatch/Clinical Trials/NCT06108050
JZP898 Intravenous Infusion as Monotherapy and Combination With Pembrolizumab in Adults With Advanced/Metastatic Solid Tumors
Is NCT06108050 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including JZP898 and Pembrolizumab for advanced solid tumor.
Treatment: JZP898 · Pembrolizumab — This Phase 1 first-in-human study will investigate the safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary antitumor activity of JZP898 monotherapy as well as JZP898 in combination with pembrolizumab in adult participants with advanced or metastatic solid tumors.
Check if I qualifyExtracted eligibility criteria
Cancer type
Tumor Agnostic
Biomarker criteria
Allowed: BRAF V600 mutation
Melanoma with known BRAFv600 mutation: received BRAF/MEKi therapy before this study.
Allowed: MLH1 MSI-H
CRC [MSI-H]
Disease stage
Required: Stage IV
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: platinum-based chemotherapy — NSCLC, HNSCC
NSCLC: eligible for platinum-based therapy and received platinum-based therapy prior to inclusion in the study. HNSCC: eligible for platinum therapy and received platinum-based therapy prior to inclusion in this study.
Must have received: BRAF inhibitor — Melanoma with known BRAFv600 mutation
Melanoma with known BRAFv600 mutation: received BRAF/MEKi therapy before this study.
Must have received: checkpoint inhibitor — NSCLC, HNSCC, melanoma, RCC, and UC (Parts A2 and B)
previously-treated (≥ 1 line of prior anticancer therapy) participants with select tumor types (NSCLC, HNSCC, melanomas, RCC, and UC) who have progressed on/after prior CPI therapy
Cannot have received: IFNα therapy
Receipt of prior IFNα therapy
Cannot have received: anticancer therapy
Exception: within 5 half-lives or 4 weeks (whichever is shorter) prior to the first dose of study drug
Received any anticancer therapy within 5 half-lives or 4 weeks (whichever is shorter) prior to the first dose of study drug
Cannot have received: radiotherapy
Exception: within 2 weeks of the first dose of study drug or have had a history of radiation pneumonitis
Received prior radiotherapy within 2 weeks of the first dose of study drug or have had a history of radiation pneumonitis
Lab requirements
Blood counts
Adequate organ and bone marrow function as indicated by the following laboratory values (within 4 weeks prior to starting the study interventions)
Kidney function
Adequate organ and bone marrow function as indicated by the following laboratory values (within 4 weeks prior to starting the study interventions)
Liver function
Adequate organ and bone marrow function as indicated by the following laboratory values (within 4 weeks prior to starting the study interventions)
Adequate organ and bone marrow function as indicated by the following laboratory values (within 4 weeks prior to starting the study interventions)
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- California Cancer Associates for Research and Excellence · Encinitas, California
- California Cancer Associates for Research and Excellence · Fresno, California
- Sarah Cannon Research Institute at HealthONE · Denver, Colorado
- Florida Cancer Specialists · Orlando, Florida
- Duke University Medical Center - Duke Cancer Institute · Durham, North Carolina
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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