ANG-3070 in Healthy Adult Participants

NCT ID: NCT04196179

Last Updated: 2021-07-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 97 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-12-17
• Study Completion Date: 2021-03-10

Brief Summary

This is a Phase 1 study, to assess the safety, tolerability, pharmacokinetics, and food effect of single and multiple ascending doses of ANG-3070 in healthy adult participants.

This study is comprised of 12 cohorts. 5 single ascending dose (SAD) cohorts 6multiple ascending dose (MAD) cohorts, and 1 single dose food effect (FE) cross-over cohort Each cohort will have a total of 8 subjects: SAD and MAD (2 subjects receiving placebo and 6 subjects receiving active ANG-3070)

Detailed Description

This is a Phase 1 study, to assess the safety, tolerability, pharmacokinetics, and food effect of single and multiple ascending doses of ANG-3070 in healthy adult participants.

Each cohort will have a total of 8 subjects: SAD and MAD (2 subjects receiving placebo and 6 subjects receiving active ANG-3070). The study design employs sentinel dosing with 2 subjects (1 placebo, 1 active treatment) at least 24 hours prior to remainder of cohort for dose cohort 1.

SAD cohorts are defined as follows, with the FE crossover occurring for participants in cohort A3 on Day 15 and in cohort D1 on Day 5:

A1 ANG-3070 50 mg (n=6) / Placebo (n=2) A2 ANG-3070 100 mg (n=6) / Placebo (n=2) A3 ANG-3070 200 mg (n=6) / Placebo (n=2) A3 Day 15ANG-3070 200mg (n=6) / Placebo (n=2) A4 ANG-3070 400 mg (n=6) / Placebo (n=2) A5 Day 1 ANG-3070 600 mg (n=6) / Placebo (n=2) D1 Day 1 ANG-3070 600 mg Single Dose (n=6) / Placebo (n=2) D1 Day 5 (ANG-3070 600 mg Single Dose (n=6) / Placebo (n=2)

MAD cohorts will receive drug or placebo twice daily for 14 consecutive days (Day 1 to Day 14) or drug or placebo once daily for 14 consecutive days (Day 1 to Day 14) as follows:

B1 ANG-3070 50 mg BID (n=6) / Placebo (n=2) B2 ANG-3070 100 mg BID (n=6) / Placebo (n=2) B3 ANG-3070 250 mg BID (n=6) / Placebo (n=2) B4 ANG-3070 500 mg BID (n=6) / Placebo (n=2) C1 ANG-3070 400 mg QD (n=6) / Placebo (n=2) C2 ANG-3070 600 mg QD (n=6) / Placebo (n=2)

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

SAD

A1 Day 1 ANG-3070 50 mg (n=6) / Placebo (n=2) Oral

A2 Day 1 ANG-3070 100 mg (n=6) / Placebo (n=2) Oral

A3 Day 1 ANG-3070 200 mg (n=6) / Placebo (n=2) Oral

Day 15 ANG-3070 200mg (n=6) / Placebo (n=2) Oral

A4 Day 1 ANG-3070 400 mg (n=6) / Placebo (n=2) Oral

A5 Day 1 ANG-3070 600 mg (n=6) / Placebo (n=2) Oral

D1 Single Dose Food Effect: Day 1 ANG 3070 600 mg *with and without food* (n=6)/ Placebo (n=2) Oral

Group Type: EXPERIMENTAL

ANG3070

Intervention Type: DRUG

ANG-3070 drug product is a an immediate release oral solid. The drug product consists of a Size 00 Swedish orange capsule containing drug substance (10 mg, 50 mg, or 250 mg) with no excipients.

Placebo oral capsule

Intervention Type: DRUG

ANG-3070 placebo capsules visually match the drug product.

MAD

B1 ANG-3070 50 mg BID (n=6) / Placebo (n=2)

B2 ANG-3070 100 mg BID (n=6) / Placebo (n=2)

B3 ANG-3070 250 mg BID (n=6) / Placebo (n=2)

B4 ANG-3070 500 mg, BID (n=6)/ Placebo (n=2)

C1 ANG-3070 400 mg, QD(n=6)/ Placebo (n=2)

C2 ANG-3070 600 mg, QD (n=6)/ Placebo (n=2)

Group Type: EXPERIMENTAL

ANG3070

Intervention Type: DRUG

ANG-3070 drug product is a an immediate release oral solid. The drug product consists of a Size 00 Swedish orange capsule containing drug substance (10 mg, 50 mg, or 250 mg) with no excipients.

Placebo oral capsule

Intervention Type: DRUG

ANG-3070 placebo capsules visually match the drug product.

Interventions

ANG3070

ANG-3070 drug product is a an immediate release oral solid. The drug product consists of a Size 00 Swedish orange capsule containing drug substance (10 mg, 50 mg, or 250 mg) with no excipients.

Intervention Type: DRUG

Placebo oral capsule

ANG-3070 placebo capsules visually match the drug product.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy male or female volunteers, aged 18 to 65 years (inclusive at the time of informed consent);

2. Participants must be in good general health, with no significant medical history, have no clinically significant abnormalities on physical examination at Screening and/or before administration of the initial dose of study drug; and

3. Participants must have a minimum body weight of 50 kg and a Body Mass Index (BMI) between ≥18.0 and ≤32.0 kg/m2 at Screening;

Exclusion Criteria

1. Pregnant or lactating at Screening or planning to become pregnant (self or partner) at any time during the study, including the follow-up period;

2. Prior or ongoing medical conditions, medical history, physical findings, or laboratory abnormality that, in the Investigator's (or delegate's) opinion, could adversely affect the safety of the participant;

3. History of gastrointestinal (GI) disorders such as celiac disease, atrophic gastritis, lactose intolerance, and Helicobacter (H.) pylori infection;

4. Presence of any underlying physical or psychological medical condition that, in the opinion of the Investigator, would make it unlikely that the participant will comply with the protocol or complete the study per protocol;

5. Any surgical or medical condition that could interfere with the absorption, distribution, metabolism, or excretion of the study drug;

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Angion Biomedica Corp

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Shakil Aslam, MD

Role: STUDY_DIRECTOR

Angion Biomedica

Locations

Nucleus Network, VIC

Melbourne, , Australia

Countries

Australia

Other Identifiers

ANG-3070-001

Identifier Type: -

Identifier Source: org_study_id