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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04883125
Other study ID # MD/17.12.30
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date January 1, 2018
Est. completion date April 15, 2021

Study information

Verified date May 2021
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessment of patients response and expression levels of CITED2 and HIF2a genes on adding pioglitazone to imatinib therapy.


Description:

Eligible denovo CML patients will be treated by combination drug therapy of imatinib 400 mg plus pioglitazone (15 - 30mg).They will be on follow up for their complete blood count (CBC), chemistry profile and random blood sugar every 2 weeks. After 3, 6 and 12 months of treatment the patients response will be evaluated and compared with the obtained responses of a historical control group. Assessment of the hypoxia induced factor 2 alpha (HIF2a) gene and CBP/p300-interacting transactivator with glutamic acid (E) and aspartic acid (D)-rich tail 2 (CITED2) gene expression levels before and after 6 months of treatment will be additionally evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date April 15, 2021
Est. primary completion date April 15, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - CML cases (BCR-ABL1 positive) Exclusion Criteria: - Accelerated or blastic crisis - Atypical CML (BCR-ABL1 negative) - Chronic myelomonocytic leukemia (CMML) - Pregnant or breastfeeding females. - Patients with severe organ dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Pioglitazone 15mg
pioglitazone (7.5-30 mg) once daily plus imatinib 400 mg 6 months

Locations

Country Name City State
Egypt Faculty of Medicine Mansoura Dakahlia

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of major molecular response(MMR) at 12 months Percentage of patients obtaining MMR at 12 months 1 year
Primary Impact of treatment on the expression levels of stemness genes Follow up the expression of CITED2 and HIF2a genes pattern 6 months
Secondary Impact of treatment on the rate of transformation Progression into accelerated or blastic phases 1 years
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