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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.

Phase 1RecruitingJazz PharmaceuticalsNCT06108050Data as of May 2026

Treatment: JZP898 · PembrolizumabThis 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.

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Extracted 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

Min 1 prior line

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

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