A Study Evaluating the Safety, Efficacy, and Pharmacokinetics (PK) of EVOLVE104 in Participants With Advanced Urothelial and Squamous Cell Carcinomas

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A Study Evaluating the Safety, Efficacy, and Pharmacokinetics (PK) of EVOLVE104 in Participants With Advanced Urothelial and Squamous Cell Carcinomas

Status
Active
Cancer Type
Anal Cancer
Bladder Cancer
Cervical Cancer
Esophogeal Cancer
Lung Cancer
Penile Cancer
Urethral Cancer
Trial Phase
Phase I
Eligibility
18 Years and older (Adult, Older Adult ), Male and Female
Study Type
Treatment
NCT ID
NCT07217171
Protocol IDs
EIU-104101 (primary)
Drug: EVOLVE104
Study Sponsor
EvolveImmune United, Inc

Summary

The goal of this study is to evaluate the safety and effectiveness of EVOLVE104 in participants with advanced urothelial and squamous cell carcinomas who have previously taken standard treatment options, have declined or have been ineligible for treatment with these medications. Participants with advanced or metastatic cancer who meet all eligibility criteria may be eligible to participate in the study.

Eligibility

Key Inclusion Criteria:

Participants must have locally advanced or metastatic cancer with one of the following tumor types: bladder cancer, squamous cell carcinoma of the lung, esophagus, skin, or an anogenital squamous cell carcinoma.

  1. Participant must have documented disease progression during or post treatment with standard of care, dependent upon tumor type.
  2. The cancer must be measurable by CT scan or MRI.
  3. Eastern Cooperative Oncology Group (ECOG) performance status score ≤1.
  4. Anticipated life expectancy of at least 3 months.
  5. Adequate organ function, as indicated by standard blood tests.
  6. Able to provide a fresh or archival tumor biopsy.
  7. Male and female participants must agree to use contraception during the study and for 120 days after the last dose of study drug, except for women who are post-menopausal or surgically sterile.

Key Exclusion Criteria:

  1. The participant is a candidate for treatment with a targeted agent known to provide a benefit.
  2. Persistent significant toxicities from prior anticancer therapy.
  3. Brain metastases unless previously treated and stable.
  4. Prior severe or life-threatening immunologic reactions to previous therapies.
  5. Significant medical conditions, including but not limited to:

    • History of clinically significant cardiac disease
    • Severe esophageal disease such as esophageal rupture or severe erosive esophagitis.
    • Active inflammatory corneal or conjunctival inflammation, erosion, or ulcerations.
    • History of cirrhosis or significant portal hypertension.
    • Uncontrolled or significant infection.
    • History of certain other cancers in the past 3 years.
    • History of arterial thrombosis, stroke and transient ischemic attack within 6 months.
    • Active or uncontrolled HIV, HBV or HCV infection.
    • Autoimmune or other condition requiring chronic systemic immunosuppression.

Treatment Sites in Georgia

Winship Cancer Institute of Emory University


1365 Clifton Road NE
Building C
Atlanta, GA 30322
winshipcancer.emory.edu

**Clinical trials are research studies that involve people. These studies test new ways to prevent, detect, diagnose, or treat diseases. People who take part in cancer clinical trials have an opportunity to contribute to scientists’ knowledge about cancer and to help in the development of improved cancer treatments. They also receive state-of-the-art care from cancer experts... Click here to learn more about clinical trials.