A Study of PHST001 in Advanced Solid Tumors

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This is a multi-center, first-in-human (FIH), open-label, Phase 1a/1b dose escalation and dose expansion study to assess the safety, PK, pharmacodynamics, and antitumor activity of PHST001 monotherapy (Phase 1a) or in combination with chemotherapy (Phase 1b) in adult participants with advanced relapsed and/or refractory solid tumors (including but not limited to CNS tumors in Phase 1a only). In Phase 1b cohort expansions, the study will focus on participants with advanced relapsed and/or refractory ovarian cancer, endometrial cancer, and cholangiocarcinoma. The study's primary objective is to evaluate the safety and tolerability of PHST001 and determine the RP2D (Recommended Phase 2 dose) of PHST001 monotherapy and in combination with chemotherapy as well as assess the anti-tumor activity of PHST001 and chemotherapy in Phase 1b.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Potwierdzony zaawansowany nowotwór, który nie reaguje na dostępne standardowe leczenie
  • Wystarczająca funkcja narządów wewnętrznych
  • Możliwość zapobiegania ciąży podczas badania
  • Widoczny guz mierzalny w badaniach obrazowych
  • Dobry stan ogólny (skala ECOG 0-1)

✗ Disqualifies

  • Niedostateczna odporność (immunodeficyt)
  • Przebyte inne nowotwory (z wyjątkami jak białaczka skóry lub rak prostaty we wczesnym stadium)
  • Przerzuty do mózgu, które aktywnie się rozwijają lub wymagają sterydów
  • Leczenie innym lekiem przeciwnowotworowym w ciągu ostatnich 3 tygodni
  • Poważne skutki uboczne z poprzedniego leczenia, które nie ustąpiły

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 12, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (20)

Precision NextGen Oncology & Research Center

Beverly Hills, United States

USC Norris Comprehensive Cancer Center

Los Angeles, United States

Stanford University School of Medicine

Palo Alto, United States

Sarah Cannon Research Institute (SCRI) Oncology Partners - Denver Health One

Denver, United States

Yale Cancer Center

New Haven, United States

University of Chicago Medical Center

Chicago, United States

Dana Farber Cancer Institute

Boston, United States

University of Michigan Rogel Cancer Center

Ann Arbor, United States

START Center for Cancer Research - Midwest

Grand Rapids, United States

START Center for Cancer Research - Long Island New York

Lake Success, United States

Mount Sinai

New York, United States

Duke Cancer Institute

Durham, United States

Sarah Cannon Research Institute (SCRI) Oncology Partners

Nashville, United States

Vanderbilt-Ingram Cancer Center

Nashville, United States

START Center for Cancer Research - Texas

Fort Worth, United States

MD Anderson Cancer Center

Houston, United States

NEXT Oncology - Dallas

Irving, United States

START Center for Cancer Research - San Antonio

San Antonio, United States

University of Texas (UT) Health

San Antonio, United States

NEXT Oncology - Virginia

Fairfax, United States

Trial contact

Andrew Ferguson/VP Clinical Development, PhD

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/13/2026.

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