Status:
COMPLETED
First in Human Study of RVP-001, a New Manganese Based MRI Contrast Agent
Lead Sponsor:
Reveal Pharmaceuticals Inc.
Collaborating Sponsors:
National Cancer Institute (NCI)
Quotient Sciences
Conditions:
Healthy
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
The objectives of this trial are: 1. To evaluate the safety and tolerability of single ascending doses of RVP-001 in healthy adult volunteers 2. To determine the pharmacokinetics and elimination of R...
Detailed Description
The first in human study is intended to evaluate the safety and tolerability of single ascending doses of RVP-001 in healthy adult volunteers, and to determine the pharmacokinetics and elimination of ...
Eligibility Criteria
Inclusion
- Male or female subjects
- Healthy subjects aged 18 to 55 years inclusive
- Suitable veins for phlebotomy, cannulation, or repeated venipuncture
- Have a body mass index between 18 and 32 kg/m\^2 (inclusive); weigh at least 55 kg.
- Appropriately completed written informed consent prior to any study specific procedures.
Exclusion
- Any clinically significant abnormality or abnormal laboratory test results found during medical screening
- Vital sign abnormalities at screening or admission
- History of clinically significant cardiovascular, renal, hepatic, chronic respiratory or gastrointestinal disease; neurological or psychiatric disorder, as judged by the investigator
- Positive pregnancy test at screening or admission
- History of alcohol abuse
- History of drug abuse
- Use of nicotine-containing products within 12 months of study start
- Use of medication except topical products without significant systemic absorption
- Known allergies to any component of RVP-001
- Subjects who have received any investigational product (IP) in a clinical research study within 5 IP half-lives or 30 days prior to first dose.
- Donation of plasma within 7 days prior to dosing; significant donation or loss of blood within 30 days prior to the first dosing.
- Any reason which, in the opinion of the Principal Investigator, would prevent the subject from participating in the study.
Key Trial Info
Start Date :
May 18 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 22 2022
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT05413668
Start Date
May 18 2022
End Date
August 22 2022
Last Update
April 22 2025
Active Locations (1)
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1
Quotient Sciences
Miami, Florida, United States, 33126