Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Amisodin in Healthy Adult Subjects With Amyotrophic Lateral Sclerosis

NCT07221240 | Recruiting Phase 1 FDA Drug

• 1 other identifier: PRG-A-001
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 1

Brief Summary

Researchers will evaluate the safety, tolerability, and pharmacokinetics (PK) of orally administered Amisodin in healthy adult subjects through a randomized, double-blind, placebo-controlled Phase 1 study consisting of two parts: single ascending dose (SAD) and multiple ascending dose (MAD). The food effect will be assessed in one cohort in Part1. Approximately 48 healthy, adult subjects are planned to be enrolled in total. Subjects will participate in only one part and one cohort.

Conditions

Amyotrophic Lateral Sclerosis

Outcome Measures

Primary Outcomes (1)

• Number and severity of TEAEs following a single oral dose of Amisodin and placebo.

  To evaluate the safety and tolerability of a single ascending dose of Amisodin in healthy adult subjects.

  From signing of the informed consent form until the follow-up visit (7 days [± 1 day] after dosing).

Secondary Outcomes (20)

• Pharmacokinetics (PK) of Amisodin

  SAD- Day 1 to Day 4 MAD- Day 1

• Pharmacokinetics (PK) of Amisodin

  SAD- Day 1 to Day 4

• Pharmacokinetics (PK) of Amisodin

  SAD- Day 1 to Day 4

• Pharmacokinetics (PK) of Amisodin

  SAD- Day 1 to Day 4

• Pharmacokinetics (PK) of Amisodin

  SAD- Day 1 to Day 4 MAD- Day 1

Study Arms (2)

Drug: Amisodin

EXPERIMENTAL

Subjects who have successfully completed the screening phase will enter the treatment phase of the study and be randomized to a treatment arm. Subjects randomized to the Amisodin arm will receive orally administered Amisodin either as a single ascending dose (SAD) or multiple ascending doses (MAD) under fasting conditions, with one cohort in the SAD part crossing over to receive the same dose under fed conditions to assess the effect of food.

Drug: Amisodin

Drug: Placebo

PLACEBO COMPARATOR

Subjects who have successfully completed the screening phase will enter the treatment phase of the study and be randomized to a Placebo arm. Subjects randomized to the Placebo arm will receive orally administered Placebo either as a single ascending dose (SAD) or multiple ascending doses (MAD) under fasting conditions.

Other: Placebo

Interventions

Amisodin DRUG

Administered as specified in the treatment arm.

Drug: Amisodin

Placebo OTHER

Administered as specified in the Placebo arm.

Drug: Placebo

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• \. Healthy, adult, male or female (of non-childbearing potential only)\*, 18 55 years of age, inclusive, at the screening visit.
• Females of non-childbearing potential are defined as follows:
• Females who have undergone one of the following sterilization procedures at least 6 months prior to the first dosing:
• o Hysteroscopic sterilization
• o Bilateral tubal ligation or bilateral salpingectomy
• o Hysterectomy
• Bilateral oophorectomy or
• Females who are postmenopausal with amenorrhea for at least 1 year prior to the first dosing and have follicle-stimulating hormone (FSH) serum levels consistent with postmenopausal status. 2. Male subjects must follow protocol specified contraception guidance as described in Section 7.4.5 Contraception Requirements and agree to refrain from sperm donation until 90 days after the last dosing. 3. Continuous non-smoker who has not used nicotine-containing products for at least 3 months prior to the first dosing based on subject self-reporting.
• \. Body mass index (BMI) ≥ 18.0 and \< 32.0 kg/m2 at the screening visit. 5. Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, or vital signs, as deemed by the PI or designee at the screening visit, including the following:
• Seated blood pressure is ≥ 90/50 mmHg and ≤ 140/90 mmHg
• Liver function tests at or below limit or normal range
• Estimated glomerular filtration rate (estimated by Modification of Diet in Renal Disease Study equation \[MDRD\] method) ≥ 90 mL/min/1.73 m² 6. No ECG findings of clinical significance as judged by the PI or qualified designee at the screening visit and at first check in, including each criterion as listed below:
• Normal sinus rhythm (heart rate between 40 and 100 bpm, inclusive)
• QTcF interval ≤ 450 msec (males) or ≤ 460 msec (females)
• QRS interval \< 110 msec; if \> 110 msec, result will be confirmed by a manual over read

You may not qualify if:

• Subjects must not be enrolled in the study if they meet any of the following criteria:
• \. Is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study.
• \. History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI or designee. 3. History of any illness that, in the opinion of the PI or designee, might confound the results of the study or poses an additional risk to the subject by their participation in the study. 4. History or presence of alcohol or drug abuse within the past 2 years prior to the first dosing. 5. History or presence of hypersensitivity or idiosyncratic reaction to compounds related to the study drug, study drug excipients, or antihistamines.
• \. Allergy to band aids, adhesive dressing, or medical tape. 7. Female subjects of childbearing potential. 8. Female subject with a positive pregnancy test at the screening visit or at first check-in or who is lactating. 9. Positive urine drug or serum alcohol results at the screening visit or first check-in. 10. Positive results at the screening visit for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV). 11. Unable to refrain from or anticipates the use of:
• Any drugs, including prescription and non-prescription medications, herbal remedies, or vitamin supplements beginning 14 days prior to the first dosing.
• Any drugs known to be significant inducers of cytochrome P450s (CYP) and/or P-glycoprotein (P-gp), including St. John's Wort, for 28 days prior to the first dosing.
• Any drugs that prolong the QT/QTc interval within 14 days (or 5 half lives, whichever is longer) prior to the first dosing.
• \. Has been on a diet incompatible with the on-study diet, in the opinion of the PI or designee, within the 30 days prior to the first dosing. 13. Donation of blood or significant blood loss within 56 days prior to the first dosing. 14. Plasma donation within 7 days prior to the first dosing 15. Participation in another clinical study within 90 days prior to the first dosing.
• The 90-day window will be derived from the date of the last blood collection or dosing, whichever is later, in the previous study to Day 1 of the current study.
• \. Any other reason determined by the PI or designee, in their opinion, that would prevent the subject's participation in the study.

Sponsors & Collaborators

• PRG Science & Technology Co., Ltd.: lead

Study Sites (1)

Pharmaron, Inc.

Baltimore, Maryland, 21201, United States

RECRUITING

MeSH Terms

Conditions

Amyotrophic Lateral Sclerosis

Condition Hierarchy (Ancestors)

Spinal Cord Diseases; Central Nervous System Diseases; Nervous System Diseases; Motor Neuron Disease; Neurodegenerative Diseases; TDP-43 Proteinopathies; Neuromuscular Diseases; Proteostasis Deficiencies; Metabolic Diseases; Nutritional and Metabolic Diseases

Central Study Contacts

Claudia Jang

CONTACT

+82 051-583-8703; claudiajang@kcrnresearch.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: CARE PROVIDER
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: The study includes SAD, MAD and a food effect cohort. While the overall study uses a parallel design, the food effect cohort is conducted using a crossover design.

Study Record Dates

• First Submitted: September 30, 2025
• First Posted: October 27, 2025
• Study Start: October 1, 2025
• Primary Completion (Estimated): May 27, 2026
• Study Completion (Estimated): July 3, 2026
• Last Updated: March 5, 2026

Record last verified: 2026-03

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)