Clinical Trials in the USA / NCT07270783
Active, not recruiting
Phase 1
Healthy Volunteer Study
NCT07270783 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Healthy Volunteer
Study summary
Double Blinded Healthy Volunteer study evaluating D-2570 against placebo in various doses.
Eligibility
Inclusion Criteria:
* Healthy volunteer subjects meeting eligibility criteria
Exclusion Criteria:
* Subjects with ongoing or history of disease or co-morbidities as assessed by Principal Investigator which would make them ineligible for the study
* Subjects with a history of drug and alcohol abuse
* Subjects taking medications, over the counter or herbal remedies
Primary outcome measure(s)
- Incidence of adverse events — From Informed Consent through study completion, an average of 48 days
Incidence of adverse events - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
Tmax - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
Cmax - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
t1/2 - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
MRT - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days.
AUC0-∞ - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
AUC0-t - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
CL/F - Result of Pharmacokinetic endpoint — From Randomization through study completion, an average of 20 days
Vz/F
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Pharmaron | Baltimore | Maryland |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07270783 on ClinicalTrials.gov ↗ ← All trials in the USA