Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:44 AM
Ignite Modification Date:
2025-12-25 @ 2:44 AM
NCT ID:
NCT04667533
Eligibility Criteria:
Inclusion Criteria:
1. Diagnosis of non-myeloid malignancy.
2. Ability to comprehend and willingness to sign a written ICF for the study.
3. Male and Female patients at least 18 years old at the time of signing the ICF.
4. Anemia caused by cancer treatment (chemotherapy) defined as Hb ≤11.0 g/dL at screening.
5. Subjects with eGFR \>60 mL/min/1.73 meter sequre at screening.
6. Weight should be ≥50 kg.
7. Willingness to participate after informed consent.
8. Females will not be pregnant or lactating, and females of childbearing potential and males will agree to use contraception.
9. Ability to swallow and retain oral medication.
Exclusion Criteria:
1. Known hypersensitivity to Desidustat and excipients in the investigational drug product.
2. History or presence of significant alcoholism, smoking or drug of abuse within 30 days at the time of screening.
3. History of RBC transfusion \<4 weeks prior enrollment.
4. History or presence of any clinically significant electrocardiogram abnormalities during screening.
5. Cardiovascular risks, such as myocardial infarction, stroke, heart failure or thromboembolic event (e.g., deep vein thrombosis (DVT) or pulmonary embolism) within previous 6 months of screening
6. Major illness and/or major surgery in the last 3 months.
7. Planned elective surgery during the study
8. Receiving or has received any investigational drug within the 30 days before receiving Desidustat.
9. Any participants with poor peripheral venous access.
10. A positive test result for Human Immunodeficiency Virus (HIV), hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibody at screening visit.
11. Female patients with following criteria will not be recruited:
* History of pregnancy or lactation in the past 3 months
* Fertile female volunteers not protected against pregnancy by adequate long-term antifertility measures
* History of less than 1 year of menopause and not using adequate long-term anti-fertility measures
* Using hormone replacement therapy
* Unable to give assurance for protection against pregnancy for 3 months after the participation in this trial
* Positive serum β-hCG level at the screening visit
12. Abnormal baseline laboratory investigations as follows:
* WBC count ≤ 3 x 103/uL
* Platelets count ≤ 100 x 103/uL
* Bilirubin ≥ 1.5 mg/dL
* ALT and/or AST ≥ 2.5 times of the ULN.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT04667533
Study Brief:
Protocol Section:
NCT04667533