RecruitingSelected Types of Solid Tumor
Evaluate the Safety, Tolerability, and Preliminary Efficacy of EVM14 Alone and in Combination in Patients With Selected Solid Tumors
Eligible age
18+ yrs
Accepts
All genders
Locations
3 states
Healthy volunteers
No
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About this study
Brief Summary: The purpose of this clinical trial is to evaluate the safety, tolerability, preliminary efficacy, and immunogenicity of EVM14 administered intramuscularly (IM) alone and in combination with pembrolizumab in patients with selected solid tumors.
Sponsor: Everest Medicines (Beijing) Co., Ltd.
You may qualify if…
- ✓ 1. Selected types of solid tumor that are pathologically confirmed unresectable advanced, recurrent, or metastatic.
- ✓ 2. Patients with at least 1 evaluable lesion assessed by Investigators within 28 days prior to the first dose of study treatment as defined per RECIST v1.1.
- ✓ 3. Eastern Cooperative Oncology Group performance status (ECOG PS) 0 or 1 at Screening.
- ✓ 4. Life expectancy ≥ 3 months.
- ✓ 5. Patients must have adequate organ function.
- ✓ 6. At screening, patients must agree to provide, if available, tumor tissue for biomarker analysis. When archival tumor tissue is not available, it is optional for the patient to undergo a fresh biopsy to collect tumor tissue if deemed medically safe by the Investigator.
You may not qualify if…
- ✕ 1. Has disease that is suitable for local treatment administered with curative intent.
- ✕ 2. Has a diagnosed and/or treated additional malignancy within 5 years prior to the first dose of study treatment except for: curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, and curatively resected in situ breast, cervical cancer, and prostate cancer.
- ✕ 3. Histologically/cytologically confirmed nasopharynx cancer. Has non-squamous histology NSCLC. If small cell elements are present, the patient is ineligible.
- ✕ 4. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
- ✕ 5. Has a diagnosis of immunodeficiency.
- ✕ 6. Use of systemic corticosteroid (\> 10 mg/day prednisone or equivalent) or other immunosuppressive medication within 14 days before the first dose of study treatment.
- ✕ 7. Has active autoimmune disease that has required systemic treatment in past 2 years or history of autoimmune disease that has possibility of relapse or at risk of having these conditions.
- ✕ 8. Poorly controlled co-morbidity, including but not limited to poorly controlled hypertension (systolic blood pressure ≥ 160 mmHg and/or diastolic blood pressure ≥ 100 mmHg) and poorly controlled type 2 diabetes, or other serious conditions requiring systemic treatment. Active gastric or duodenal ulcer.
Where it's recruiting
Source: ClinicalTrials.gov · NCT07095868 · last updated 2026-08-04