Safety, Tolerability, and Pharmacokinetics Study of ATH-1020

Healthy Volunteers Clinical Trial

Official title:

A Randomized, Placebo-Controlled, Double-Blinded, First-in-Human, Adaptive Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses (Part A) and Multiple Ascending Doses (Part B) of Orally Administered ATH-1020 in Healthy Young and Elderly Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05169671
• Other study ID #: ATH-1020-0101
• Status: Completed
• Phase: Phase 1
• Start date: March 30, 2022
• Est. completion date: September 9, 2022

Study information

• Verified date: April 2024
• Source: Athira Pharma
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This Phase 1 randomized, placebo-controlled, double-blinded, first-in-human study will evaluate safety, tolerability, and pharmacokinetics of single and multiple ascending doses of ATH-1020 in healthy young and elderly subjects.

Description:

This is a Phase 1 first-in-human, 2-part adaptive study. Both Part A and Part B will be performed in a randomized, placebo-controlled, and double-blind manner.

Part A - Single Ascending Dose (SAD) Part A will be a SAD study investigating multiple dose levels of ATH 1020.

Part B - Multiple Ascending Dose (MAD) Part B will be a multiple ascending dose (MAD) study investigating multiple dose levels of ATH-1020.

Subjects in Cohort B5 (4 subjects) will additionally undergo CSF sampling pre-dose on Day 4 and up to 3 post dose timepoints to evaluate ATH-1020 blood-brain-barrier penetration

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: September 9, 2022
• Est. primary completion date: September 9, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

All Subjects

1. Body mass index (BMI) of = 18.0 and = 32.0 kg/m2 at Screening, with minimum weight of 60 kg.

2. Subjects in generally good health per the investigator's discretion.

3. Male subjects and their partners must be willing to comply with the contraceptive requirements of the study.

4. Subjects must have adequate venous access.

Part A (SAD)

5. Male subjects aged 18 to 50 years at the time of signing the informed consent.

Part B (MAD)

6. Male subjects aged 18 to 50 years (Cohorts B1, B2, B3, and B5); male and post-menopausal female subjects aged 65 to 85 years (Cohort B4) at the time of signing the informed consent.

Exclusion Criteria:

1. History of significant drug allergies (including to any excipients) or of anaphylactic reaction.

2. Any condition per the investigator's discretion, which while not requiring chronic medication use, is likely to require intermittent/acute therapeutic intervention.

3. Any history of seizures or loss of consciousness for an unknown reason.

4. History of or positive results of serology screening for hepatitis B, hepatitis C or human immunodeficiency virus (HIV).

5. Abnormal liver tests

6. Impaired renal function.

7. History of having taken another investigational drug within 30 days prior to Admission (Day -1).

8. Major surgery within 90 days prior to Admission (Day -1) or anticipated surgery during the study.

Part A (SAD)

9. Female subjects are not permitted.

10. Any medical condition that requires chronic medication use.

Part B (MAD)

11. A history of intermittent benzodiazepine (short-acting only) or other treatments for insomnia and anxiety are allowed, provided that the subject is able to abstain from their use during the Screening period, and from Admission until discharge from the study.

12. Reported changes in cognition and reported history of declines in everyday life in the last year.

Part B (MAD) CSF Sampling (Cohort B5)

13. Subject history of or current contraindication to lumbar puncture/spinal catheterization.

14. Clinically significant abnormalities in coagulation parameters.

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• ATH-1020
ATH-1020 in oral capsule form
• Placebo
Placebo in oral capsule form

Locations

Country	Name	City	State
United States	Biotrial, Inc.	Newark	New Jersey

Sponsors (3)

Lead Sponsor	Collaborator
Athira Pharma	Alturas Analytics, Inc., Biotrial Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)	Safety and tolerability of single or multiple ascending doses of ATH-1020 as measured by vital signs and clinical laboratory measurements.	Up to 12 days post initial dosing (Part A); Up to 19 days post initial dosing (Part B)
Secondary	Maximum observed plasma concentration (Cmax)	Cmax will be determined from all collected plasma samples from baseline through up to 48 hours post-dose.	Cmax will be determined from all collected plasma samples from baseline through up to 48 hours post-dose.
Secondary	Time to maximum observed plasma concentration (Tmax)	Tmax will be determined from all collected plasma samples from baseline through up to 48 hours post-dose.	Samples collected pre-dose and at predetermined timepoints within 48 hours post-dose.
Secondary	Plasma concentration at the end of the dosing interval (Ctrough)	Ctrough will be determined from the last plasma sample prior to the following dose (cohort B only).	Samples collected pre-dose and at predetermined timepoints within 24 hours post-dose.
Secondary	Area under the plasma concentration time curve (AUC)	AUC will be determined from all collected plasma samples from baseline through up to 48 hours post-dose.	Samples collected pre-dose and at predetermined timepoints within 48 hours post-dose.
Secondary	Half-life (t1/2)	t1/2 will be determined from all collected plasma samples from baseline through up to 48 hours post-dose.	Samples collected pre-dose and at predetermined timepoints within 48 hours post-dose.
Secondary	Amount of IMP excreted unchanged in the urine (Ae)	Ae will be determined from all collected urine samples from baseline through up to 24 hours post-dose (cohort B1-4 only).	Samples collected pre-dose on Day 1 and predetermined timepoints on Day 1, 9, and 10, within 24 hours post-dose.