CompletedPhase 1NCT03884556

TTX-030 Single Agent and in Combination With Immunotherapy or Chemotherapy for Patients With Advanced Cancers

This is a phase 1/1b study of TTX-030, an antibody that inhibits CD39 enzymatic activity, leading to accumulation of pro-inflammatory adenosine triphosphate (ATP) and reduction of immunosuppressive adenosine, which may change the tumor microenvironment and promote anti-tumor immune response. This trial will study the safety, tolerability, pharmacokinetics, and anti-tumor activity of TTX-030 as a single agent and in combination with an approved anti-PD-1 immunotherapy and standard chemotherapies.

Checked against the public recordLast updated Jul 2, 2025 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 1
U.S. locations16
SponsorTrishula Therapeutics, Inc.
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Trishula Therapeutics, Inc.
Interventions being studied
Drug: TTX-030; Drug: Pembrolizumab; Drug: Gemcitabine; Drug: nab paclitaxel
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Abreviated Inclusion Criteria 1. Advanced solid tumor malignancy or relapsed/refractory lymphoma, or * eligible to receive single-agent pembrolizumab as standard of care, or * eligible to receive single-agent docetaxel as standard of care, or * advanced pancreatic adenocarcinoma and eligible to receive gemcitabine plus nab-paclitaxel as standard of care. 2. Age 18 years or older, is willing and able to provide informed consent 3. Evidence of measurable disease 4. Life expectancy \> 12 weeks and Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 Abbreviated Exclusion Criteria 1. History of allergy or hypersensitivity to study treatment components. Patients with a history of severe hypersensitivity reaction to any monoclonal antibody. 2. Use of investigational agent within 28 days prior to the first dose of study treatment and throughout the study 3. Receiving high-dose systemic steroid therapy or any other form of immunosuppressive therapy 4. History of severe autoimmune disease 5. Uncontrolled intercurrent illness or other active malignancy requiring ongoing treatment

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • UC Irvine Cancer CenterOrange, California
  • UC Davis Comprehensive Cancer CenterSacramento, California
  • University of California, San FranciscoSan Francisco, California
  • Sylvester Comprehensive Cancer CenterMiami, Florida
  • Norton Cancer InstituteLouisville, Kentucky
  • Nebraska Cancer Center Oncology Hematology West P.C.Omaha, Nebraska
  • Rutgers Cancer Institute of New JerseyNew Brunswick, New Jersey
  • Columbia University Irving Medical CenterNew York, New York
  • Memorial Sloan Kettering Cancer CenterNew York, New York
  • Montefiore Medical CenterThe Bronx, New York
  • University Hospitals Cleveland Medical CenterCleveland, Ohio
  • UPMC Hillman Cancer CenterPittsburgh, Pennsylvania

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 2, 2025. Always confirm current availability with the study team.

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