A Trial to Assess Safety, Tolerability, and Pharmacokinetics of AN01 Inhalation Powder in Healthy Participants

AirNexis Therapeutics, Inc.

Status and phase: Completed; Phase 1

Conditions: Healthy Participants Study; Healthy Volunteer

Treatments: Drug: Placebo; Drug: AN01

Study type: Interventional

Funder types: Industry

Identifiers

NCT07554365

AN-HV-1001

Details and patient eligibility

About

AN01 is a selective small-molecule dual inhibitor of phosphodiesterase 3 and 4 (PDE3/4).

As a potential new therapy for COPD, AN01 is expected to serve either as a monotherapy for COPD or as adjunctive therapy to current inhaled standard treatments, potentially generating synergistic complementary effects in patients requiring additional therapeutic options.

The primary objective of this study is to evaluate the safety, tolerability, and pharmacokinetics of multiple doses of AN01 in healthy participants.

Full description

The study is composed of three multiple ascending dose (MAD) cohorts in which participants will be randomly allocated to receive placebo or ascending doses of active AN01 in a double-blinded manner. An additional multiple ascending dose cohort may be added at Sponsor's discretion.

Enrollment: 25 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Healthy adults ≥18 and ≤60 years (inclusive).
2. Body Mass Index (BMI) ≥18 and ≤32 kg/m2 (inclusive).
3. Participants who are healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, spirometry, and electrocardiogram (ECG).
4. Non-smokers or former smokers who have quit for ≥2 years with a prior smoking history of <5 pack-years (pack-years defined as = cigarettes per day × years smoked; 1 pack = 20 cigarettes).
5. Female participants must be non-pregnant and non-lactating, and, surgically sterile, use highly effective contraceptive methods from Screening until at least 30 days after the last dose of study drug, or post-menopausal for ≥12 months.
6. Male participants must be surgically sterile, abstinent, or their partner must be surgically sterile, or if engaged in sexual relations with a woman of childbearing potential (WOCBP), the male participant and his partner must use an acceptable, highly effective contraceptive method from Screening until at least 90 days after the last dose of study drug.

Exclusion criteria

1. History of clinically significant (as per Investigator's judgment) upper respiratory disease or history of any significant pulmonary disease including, but not limited to, asthma, chronic obstructive pulmonary disease (COPD), pulmonary fibrosis, and history of previous tuberculosis exposure with positive interferon gold test (without actual infection).
2. Participants with any history of, or active, clinically significant disease (e.g., cardiovascular disease, chronic liver disease, psychiatric medical history, renal disease) that could interfere with the interpretation of the study results or compromise the health of the participant based on the judgment of the Investigator.
3. Administration of vaccines/immunizations and/or boosters within 8 days prior to first dosing or if planned during the study.
4. Any history of active infection at the time of Screening and/or within 28 days prior to first dosing.
5. Any prior participation in a study with an investigational drug or device involving a biological targeted therapy, where final administration of the investigational drug or utilization of the device occurred within 24 weeks prior to first dosing.
6. History of migraine headaches requiring prescription medication or occurring more than 2-4 times per month within the past 6 months.
7. Use of non-tobacco vaping within 12 months prior to Screening.
8. Use of any tobacco and/or inhaled marijuana product within 2 years prior to Screening.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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25 participants in 2 patient groups, including a placebo group

AN01

Experimental group

Description:

Escalating multiple doses of AN01

Treatment:

Drug: AN01

Placebo

Placebo Comparator group

Description:

Escalating doses of matching placebo

Treatment:

Drug: Placebo