Overview

A Single and Multiple Ascending Dose Study to Evaluate the Safety and Pharmacokinetics of PU-AD in Healthy Subjects

Status:
Completed
Trial end date:
2019-12-23
Target enrollment:
0
Participant gender:
All
Summary
This is a first in human Phase 1 study in two parts with healthy volunteers receiving a single dose of PU AD in three small cohorts and a multiple ascending dose in two small cohorts.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Samus Therapeutics, Inc.
Criteria
Inclusion Criteria:

1. Male or female (Women of non-child bearing potential)

2. 18 to 60 years of age for part one, >/= 60 years of age for part two

Exclusion Criteria:

1. Women of child bearing potential or Female with positive pregnancy test or who is
lactating.

2. History or presence of conditions, which in the judgment of the PI, are known to
interfere with the absorption distribution, metabolism, or excretion of drugs.

3. History or presence of conditions that may place the subject at increased risk as
determined by the PI.

4. Has taken other investigational drugs or participated in any clinical study within 30
days.

5. Any other condition or prior therapy that, in the PI's opinion, would make the subject
unsuitable for the study, or unable or unwilling to comply with the study procedures