Single Ascending-dose Study to Evaluate Safety, Tolerability, and PK of MYMD1 in Healthy Male Adult Subjects

Completed · Phase 1 · Has a placebo group

Conditions studied: Undefined

In brief

Double-blind, placebo-controlled, First-in-Human, single ascending-dose study. Approximately 40 healthy adult male subjects will be given a single capsule of MYMD1 to determine its safety, how well it is tolerated, how the body acts on the experimental drug, and how the experimental drug acts on the body. This will be based on blood and urine sample analysis and other physical measurements.

Key facts

Study ID

NCT04349761

Run by

TNF Pharmaceuticals, Inc.

People needed

40

Starts

2019-06-11

Expected to finish

2019-12-30

Last updated by the study team

2020-04-16

Who can join

Age: 18 and older, up to 65. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• Written Informed Consent.
• Stable medical history and general health.
• Body weight between 60 - 100 kg and Body Mass Index (BMI) of 18-31 kg/m2.
• Estimated GFR (eGFR) - mL/min/1.73m2 or estimated creatinine clearance (CLcr) (mL) ≥90.
• Normal hepatic function.
• Adequate peripheral venous access.
• Test negative for HIV, hepatitis C virus antibodies, and hepatitis B surface antigen (HBsAg).
• Test negative for drugs of abuse.
• Willing and able to complete all study assessments and procedures and to communicate effectively with the Investigator and study center staff.
• Willing to use effective contraception from Day -1 until 90 days after receiving study medication.

You may not qualify if…

• Allergy to any product ingredients.
• Unable to swallow capsules.
• Elective medical procedure during study.
• Abusing drugs or alcohol and/or history of drug or alcohol dependence within 6 months of study entry.
• History of seizure disorder requiring medical treatment after 18 years of age.
• Current smoker or smokeless tobacco user.
• Participation in drug or medical device clinical study within 30 days of study. entry or 5 times half-life of study drug, whichever is longer.
• Medically significant standard clinical laboratory assessments.
• Significant medical condition which might interfere with the study or put subject at significant risk.
• QTcF >450 ms or clinically significant ECG abnormalities.
• Elevation of blood pressure (BP) - Supine BP >145mmHg; Diastolic BP. >92mmHg;l heart rate (HR) >100 bpm.
• Gastrointestinal malabsorption.
• Abnormal thyroid function (TSH, T4 and/or T3 levels): elevated thyroid antibodies (anti- TPO and/or anti-Thyroglobulin); thyroid goiter, or known thyroid nodule(s) at Baseline; >Abnormal renal function (estimated GFR >90mL/min/1.73m2 or estimated creatinine clearance <90mL) and/or abnormal hepatic function at Baseline.
• Treatment with any prescription or nonprescription drugs, including vitamins, minerals, or herbal and dietary supplements, within 14 days or 5 half-lives of Day 1, whichever is longer - except Tylenol.
• Use within 30 days prior to Day 1 of any drugs or substances, including grapefruit juice, that are known to strongly inhibit or induce cytochrome P450 (CYP) enzymes.
• Donation of blood or blood product within 56 days of Day 1.

Where it is running

• Palm Beach CRO, LLC — West Palm Beach, Florida, United States

Full record on ClinicalTrials.gov

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