Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anemia of Chronic Kidney Disease
  • Chemotherapy Effect
Type
Interventional
Phase
Phase 1
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 19 years and 125 years
Gender
Both males and females

Description

A total of up to approximately 24 patients will be enrolled to receive Desidustat in an open-label manner. The study is divided into three cohorts as given below: Cohort I: Single-dose 100 mg Cohort II: Single-dose 150 mg Cohort III: Single-dose 200 mg Note:- After evaluation of PK data of 100 mg do...

A total of up to approximately 24 patients will be enrolled to receive Desidustat in an open-label manner. The study is divided into three cohorts as given below: Cohort I: Single-dose 100 mg Cohort II: Single-dose 150 mg Cohort III: Single-dose 200 mg Note:- After evaluation of PK data of 100 mg dose cohort, next cohort with higher dose will be decided. Maximum dose of Desidustat will not be exceeded than 200 mg. First cohort will be given 100 mg single dose of Desidustat. On completion of safety and PK evaluation of first cohort,the next cohort with escalated single dose (150 mg) of Desidustat will be initiated. Similar way third cohort with 200 mg single dose will be initiated after safety evaluation of 150 mg cohort data.

Tracking Information

NCT #
NCT04667533
Collaborators
Not Provided
Investigators
Study Chair: Dr Deven Parmar, MD Cadila Healthcare Ltd.