Status:
COMPLETED
Phase I Study Evaluating Safety and Tolerability of Escalating Single and Multiple Doses of of PIPE-307 and Food Effect in Healthy Volunteers
Lead Sponsor:
Contineum Therapeutics
Conditions:
Multiple Sclerosis
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
This is a randomized, double-blind study of PIPE-307 or placebo in normal healthy subjects. The study will be conducted in three parts: Part 1 will be a Single Ascending Dose (SAD) study enrolling app...
Detailed Description
This is a randomized, double-blind study of PIPE-307 or placebo given as single and multiple escalating doses in normal healthy subjects. The study will be conducted in three parts: Part 1 will be a S...
Eligibility Criteria
Inclusion
- Male or female between 18 and 55 years of age (inclusive) at time of signing informed consent.
- BMI is between 18.0 and 32.0 kg/m2
- Male or female subjects with reproductive potential agree to comply with protocol-approved double barrier contraceptive method 30 days prior to first dose and up to 90 days post last dose
- Medically healthy with no clinically significant or relevant abnormalities in medical history physical exam, vital signs, electrocardiogram (ECG), or laboratory evaluations (hematology, chemistry, and urinalysis) as assessed by the Investigator.
Exclusion
- Has a current or recurrent diseases that could affect the investigational medicinal product or affect clinical or laboratory assessments
- Experienced a significant systemic illness, as judged by the Investigator, within 30 days of the first dose
- Has a history of a significant medical, including hepatic and/or renal disease as outlined in the protocol, or psychiatric disorder that may require treatment or make the participant unlikely to fully complete the study or increase risk to the participant.
- History of alcohol or other substance abuse within the 12 months prior to dosing at the discretion of the Investigator
- Routine alcohol consumption meeting or exceeding protocol limits
- History of prior malignancy (except adequately treated non-melanoma skin cancer, carcinoma I-situ of the uterine cervix, ductal carcinoma in situ (DCIS), or localized prostate cancer
- Donated or lost more than 400ml of blood within 56 days or plasma within 14 days prior to screening
- Received an investigational agent with the last 30 days prior to dosing or within 5 half-lives of the investigational agent
- Use of any prescription medication, over-the-counter medication, vitamin or supplement, herbal or homeopathic preparations with 7 days or 5 half-lives prior to study drug administration, as determined by the Investigator. Hormone replacement therapy and hormonal contraception is permissible throughout the study
Key Trial Info
Start Date :
February 26 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2021
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT04725175
Start Date
February 26 2021
End Date
September 1 2021
Last Update
November 3 2021
Active Locations (1)
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1
Linear Clinical Research
Nedlands, Western Australia, Australia, 6009