NCT05950906CompletedPhase 1
Study to Assess PDM608 in Healthy Adult Subjects
A Two-Part Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of PDM608 in Healthy Adult Subjects
Source: ClinicalTrials.gov · Last updated 18 Nov 2025
Brief summary (registry, in English)
The purpose of this study is to assess the safety, tolerability and pharmacokinetics of PDM608 in healthy adult subjects.
- Status (registry)
- Completed
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 64 (actual)
- First submitted
- 22 May 2023
- Start date
- 27 Jun 2023
- Primary completion date
- 17 Mar 2024
- Lead sponsor
- Calibr, a division of Scripps Research
- Diseases
- Parkinson disease
- NCT number
- NCT05950906
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 64
- From 27 Jun 2023 to the primary completion date, 17 Mar 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- History of clinically significant autoimmune, cardiovascular, renal, hepatic, chronic respiratory or GI disease (except cholecystectomy), neurological or psychiatric disorder, illness/infection/hospitalization or surgical procedure within 30 days prior to first dose of study drug or any uncontrolled medical illness as judged by the investigator
- Evidence of current SARS-CoV-2 infection or exposure to confirmed infection within 10 days prior to the first dose of study drug
- Received any IMP in a clinical research study within 5 half-lives or within 30 days prior to first dose (whichever is longer)
- Taking any prescribed or over-the-counter drug or herbal remedies (other than up to 4 g per day acetaminophen and HRT) in the 14 days or 5 half-lives (whichever is longer) before IMP administration
- COVID-19 vaccine within 14 days prior to first dose or have a COVID-19 vaccine scheduled between their first dose of IMP and last dose of IMP.
- Drug or alcohol abuse in the past 2 years
- Donation of blood within 2 months or donation of plasma within 7 days prior to first dose of study medication
Other illness
- Serious adverse reaction or serious hypersensitivity to any drug or the formulation excipients
- Significant allergy requiring treatment
- Hepatitis B, Hepatitis C, HIV, TB
- Renal impairment
Other
- Have poor venous access that limits phlebotomy
- Clinically significant abnormal clinical chemistry, hematology or urinalysis
- Pregnant or lactating women or men with pregnant or lactating partners
- Regular alcohol consumption in men \>21 units per week and women \>14 units per week (1 unit = 12 oz 1 bottle/can of beer, 1 oz 40% spirit or 5 oz glass of wine)
- Positive alcohol urine test at screening or first admission
- Current and within the last six months-smokers, e-cigarettes and nicotine replacement users
- Subjects who are, or are immediate family members of, a study site or Sponsor employee
Who the study is looking for
- Healthy men, or women of non-childbearing potential
- Must agree to use an adequate method of contraception
- Body mass index (BMI) of 18.0 to 33.0 kg/m2 as measured at screening
Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Quotient Sciences-Miami, Inc Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.