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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Blinatumomab
  • 2.Take Capivasertib
  • 3.Take Nelarabine
  • +3 more
PhasePhase 1/Phase 2
DrugBlinatumomab
Routeinjection

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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