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Study details
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Trial to Test Safety of Adding Capivasertib to a Standard Leukemia Treatment Regimen

University of Chicago
NCT IDNCT07294677ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

104

Study length

about 6 years

Ages

18+

Locations

1 site in IL

What this study is about

Researchers are testing the safety of adding capivasertib to a standard leukemia treatment regimen. The trial will test different doses of capivasertib in adults with leukemia and lymphoma, along with venetoclax and chemotherapy. It aims to find the safest dose of capivasertib for this combination therapy.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Blinatumomab
  • 2.Take Capivasertib
  • 3.Take Nelarabine
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

blinatumomab, capivasertib, nelarabine, rituximab (Monoclonal antibody; targets CD20 on B-cells to destroy them), venetoclax

Drug routes

injection, intravenous, oral (Oral Tablet), injection (Injection), infusion, oral

Endpoints

Secondary: Overall survival [Cohort 2 and 3], Progression free survival [All Cohorts], Rate of CR with measurable residual disease (MRD) negativity [Cohort 1], Rate of clinical remission (CR) [Cohort 1]

Body systems

Oncology