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Study identifier: NCT07190300 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

TulmiSTAR-02: A Phase I/II Open-label Study of Tulmimetostat in Combination With Darolutamide vs. Darolutamide, and Tulmimetostat With Abiraterone in Patients With Metastatic Hormone-sensitive Prostate Cancer (mHSPC)

Condition: Metastatic Hormone-Sensitive Prostate Cancer (mHSPC)  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 1/Phase 2
Planned participants181
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of the study is to evaluate the safety, tolerability, and efficacy of the two different treatment combinations of tulmimetostat in participants with de novo or recurrent Metastatic Hormone-Sensitive Prostate Cancer (mHSPC).

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Always discuss trial participation with your own doctor first.

Locations (31)

Univ of Alabama at BirminghamBirmingham, Alabama, United StatesRecruiting
Uni Of Iowa Hospitals And ClinicsIowa City, Iowa, United StatesRecruiting
University of Kansas Cancer CenterWestwood, Kansas, United StatesRecruiting
Wichita Urology Group PAWichita, Kansas, United StatesRecruiting
Duke University Medical CenterDurham, North Carolina, United StatesRecruiting
Medical University of South Carolina MUSCCharleston, South Carolina, United StatesRecruiting
Carolina Urologic Research CenterMyrtle Beach, South Carolina, United StatesRecruiting
Huntsman Cancer InstituteSalt Lake City, Utah, United StatesRecruiting
Novartis Investigative SiteCamperdown, New South Wales, AustraliaWithdrawn
Novartis Investigative SiteWollongong, New South Wales, AustraliaRecruiting
Novartis Investigative SitePorto Alegre, Rio Grande do Sul, BrazilRecruiting
Novartis Investigative SiteMontreal, Quebec, CanadaRecruiting

+ 19 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07190300