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Study of Ipilimumab and Dasatinib Combination Therapy in Patients With Chronic or Accelerated Chronic Myeloid Leukemia

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status and phase

Withdrawn
Phase 1

Conditions

Leukemia, Myeloid, Chronic

Treatments

Biological: Ipilimumab

Study type

Interventional

Funder types

Industry

Identifiers

NCT00732186
CA184-033

Details and patient eligibility

About

The purpose of the study is to assess the safety of ipilimumab and dasatinib combination therapy in patients with CML

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ph+ CML on dasatinib therapy
  • Loss of cytogenetic or molecular response while on dasatinib therapy
  • On stable dose of dasatinib for a minimum of 12 weeks and with < 14 day interruption of treatment

Exclusion criteria

  • Blast crisis CML
  • Autoimmune disease
  • Uncontrolled or significant cardiovascular disease

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 1 patient group

Group 1 and Group 2
Experimental group
Treatment:
Biological: Ipilimumab

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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