A Phase 1 Study of the Safety and Tolerability of ICM20 in Adults (NCT05523596) | Clinical Trial Compass
CompletedPhase 1
A Phase 1 Study of the Safety and Tolerability of ICM20 in Adults
United States13 participantsStarted 2023-08-20
Plain-language summary
A Phase 1 Non-Randomized Open Label Study of Oral ICM20
Who can participate
Age range18 Years – 70 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* ≥18 to 70 years of age
* ≥125 and ≤200 pounds
* Diagnosis of chagas documented by positive serology
* No prior chagas treatment
* Able to swallow capsules and tablets
* Laboratory values:
Blood: Hemoglobin ≥9; Polymorphonuclear white blood cells \>1000; Platelets \>50,000 Liver Function Tests ≤ 2 Times Upper Limit of Normal Serum Creatinine ≤2.0 Prothrombin time, partial thromboplastin time within normal limits HemoglobinA1C \<7
* Human immunodeficiency virus negative
* Stable on current prescription medications
* Not pregnant, lactating, or planning to get pregnant
* Both men and women who are not surgically sterile, or post-menopausal, must agree to avoid pregnancy
* Willing to abstain from alcohol
* Able and willing to give informed consent
Exclusion Criteria:• Prior chagas treatment
* Known hypersensitivity to either study drug or its constituents
* Requires the continuing use of amiodarone, monoamine oxidase inhibitors, phenytoin, phenobarbital, disulfiram, anticoagulants or procoagulants, drugs or products containing alcohol or propylene glycol.
* Coagulopathy
* Glucose-6-phosphate dehydrogenase deficiency
* History, signs, or symptoms of heart failure
* History of heartburn, gastroesophageal reflux disease, or ulcers
* Unstable medical condition
* Immunodeficiency
* Requires surgery or surgical procedure within 90 days of Screening.
* Use of an investigational product within 56 days prior to baseline
* Unwilling to discontinue use of disallow…