An Open-label Dose Escalation/Expansion Trial to Evaluate the Safety and Anti-tumor Activity of TEV-56278 Alone or in Combination With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors

Last updated: March 12, 2025
Sponsor: Teva Branded Pharmaceutical Products R&D, Inc.
Overall Status: Active - Recruiting

Phase

1

Condition

Neoplasms

Treatment

Pembrolizumab

TEV-56278

Clinical Study ID

NCT06480552
TV56278-ONC-10203
  • Ages > 18
  • All Genders

Study Summary

The primary objectives of this trial are to:

  • Characterize the safety and tolerability of TEV-56278

  • Determine the Recommended Phase 2 Dose (RP2D)

  • Evaluate antitumor activity of TEV-56278

  • Determine the safety and tolerability of TEV-56278 in combination with pembrolizumab

  • Determine a RP2D of TEV-56278 in combination with pembrolizumab

The secondary objectives of this trial are to:

  • Characterize the serum pharmacokinetics of TEV-56278

  • Evaluate the antitumor activity of TEV-56278

  • Determine the safety and tolerability of TEV-56278

  • Evaluate other measures of antitumor activity of TEV-56278

  • Evaluate anti-tumor activity

Participants will be treated up to 12 months with a follow-up period of up to 12 months after last infusion. The total duration of the trial will be up to 25 months for individual participants.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Have an established histological diagnosis of selected solid tumor and must havereceived and progressed on established standard therapies or have been intolerant tosuch therapy or have been considered by the Investigator as ineligible for approvedstandard therapy

  • Have a life expectancy≥12 weeks at the time of the screening

  • Women of childbearing potential must agree to use highly effective methods ofcontraception for the course of the trial through 120 days after the last dose oftrial medication

  • Males who are sexually active with women of childbearing potential must agree to usecondoms and refrain from donating sperm for the course of the trial through 120 daysafter the last dose of trial medication

NOTE- Additional criteria apply, please contact the investigator for more information

Exclusion

Exclusion Criteria:

  • Has a history of systemic treatment therapy for cancer (including chemotherapy,immunotherapy, radiotherapy, or other investigational drug) or surgery within 4weeks prior to baseline

  • Is currently receiving or has received hematopoietic colony-stimulating growthfactors within 2 weeks before screening or transfusion support 4 weeks prior toscreening

  • Has a diagnosis of immunodeficiency

  • Has active known autoimmune disease.

  • Has a history of or known active brain metastases and/or carcinomatous meningitisand/or leptomeningeal metastasis

  • Has active or uncontrolled serious infections requiring systemic therapy within 14days prior to baseline

  • Has a history of clinically significant cardiovascular or cerebrovascular disease inprevious 6 months prior to screening

  • Has evidence of clinically significant interstitial lung disease or active,noninfectious pneumonitis

  • Has a seizure disorder requiring therapy (such as steroids or antiepileptics)

NOTE- Additional criteria apply, please contact the investigator for more information

Study Design

Total Participants: 240
Treatment Group(s): 2
Primary Treatment: Pembrolizumab
Phase: 1
Study Start date:
July 22, 2024
Estimated Completion Date:
February 25, 2031

Connect with a study center

  • Teva Investigational Site 11282

    Toronto, Ontario M5G 2M9
    Canada

    Active - Recruiting

  • Teva Investigational Site 12017

    Los Angeles, California 90025
    United States

    Active - Recruiting

  • Teva Investigational Site 12021

    Lake Mary, Florida 32746
    United States

    Active - Recruiting

  • Teva Investigational Site 12016

    Chicago, Illinois 60611
    United States

    Active - Recruiting

  • Teva Investigational Site 12015

    Detroit, Michigan 48201
    United States

    Active - Recruiting

  • Teva Investigational Site 12014

    Huntersville, North Carolina 28078
    United States

    Active - Recruiting

  • Teva Investigational Site 12058

    Pittsburgh, Pennsylvania 15232
    United States

    Active - Recruiting

  • Teva Investigational Site 12019

    Nashville, Tennessee 37203
    United States

    Active - Recruiting

  • Teva Investigational Site 12018

    Fairfax, Virginia 22031
    United States

    Active - Recruiting

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