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A Study of Pirtobrutinib in Participants With Immune Thrombocytopenia

RecruitingPhase 1/2

A Phase 1/2, Dose-finding Study Investigating the Safety and Efficacy of Pirtobrutinib in Adults With Immune Thrombocytopenia

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Have a diagnosis of primary ITP, defined as isolated thrombocytopenia not associated with another known disease process
* Have documented history of response, defined as 2 or more platelet counts greater than or equal to 50,000/microliter (μL), to at least 1 prior line of therapy. Splenectomy is considered a line of therapy
* Have relapsed or treatment-resistant primary ITP, with no available therapies known to provide clinical benefit
* Have a platelet count less than 30,000/μL on 2 occasions at least 5 days apart in the 15 days before randomization
* Have adequate liver, renal, and hematologic functions as defined by a table
* Are willing to follow contraception requirements

Exclusion Criteria:

* Have a history of any thrombotic or embolic event within 12 months before screening
* Had a transfusion with blood or blood products or plasmapheresis within 14 days (Phase 1) or within 28 days (Phase 2) of randomization
* Have significant cardiovascular disease
* Have a diagnosis or history of hematologic malignancy
* Have hepatitis B virus (HBV) defined as positive for antigen of hepatitis B (HBsAg) or polymerase chain reaction (PCR) positive for HBV deoxyribonucleic acid (DNA)
* Have hepatitis C virus (HCV) defined as positive for anti-HCV antibodies and PCR positive for HCV ribonucleic acid (RNA)

About the study

The purpose of the phase 1 part of this study was to evaluate how well pirtobrutinib is tolerated and what side effects may occur. The phase 2 part of the study will further investigate efficacy and safety of multiple pirtobrutinib dosages versus placebo.

The study drug will be administered orally in participants with Primary Immune Thrombocytopenia (ITP). Blood tests will be performed to check how much pirtobrutinib gets into the bloodstream and how long it takes the body to eliminate it.

The study will last up to approximately 16 weeks for phase 1 dose-escalation and 28 weeks for phase 2 dose-optimization, excluding screening.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 68 · Started: Jul 30, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06721013

Locations in the U.S.

CaliforniaUSC Norris Comprehensive Cancer Center, Los Angeles
Stanford University, Palo Alto
District of ColumbiaMedStar Georgetown University Hospital, Washington D.C.
FloridaUniversity of Miami Hospital and Clinics Sylvester Comprehensive Cancer Center, Miami (Not yet recruiting)
IllinoisBleeding and Clotting Disorders Institute, Peoria (Not yet recruiting)
LouisianaOchsner Clinic Foundation, New Orleans
MinnesotaMayo Clinic, Rochester
TexasTexas Oncology - Central South, Austin
MD Anderson Cancer Center, Houston
Texas Oncology Gulf Coast, The Woodlands

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.