Mosliciguat for Healthy Subjects

Age: 18 - 65
Sex: Male
Trial Phase: Phase 1
Sponsor: Pulmovant, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called mosliciguat to understand how the body absorbs, breaks down, and eliminates it. Researchers aim to ensure its safety for healthy adults. The treatment is administered in two ways: via inhaler and orally or by IV (a drip into the vein). Healthy men without lung issues such as asthma or COPD (a common lung disease) are suitable candidates for this study. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive it.

Do I have to stop taking my current medications for the trial?

The trial information does not specify if you need to stop taking your current medications. It's best to discuss this with the trial team or your doctor.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that mosliciguat, when inhaled, is generally well-tolerated by healthy adults. Three different studies found no serious side effects with once-daily inhaled doses, indicating that the body can handle the drug well without causing major health problems.

For mosliciguat taken orally or through an IV, specific safety information is not yet available. However, these forms are currently being tested in a Phase 1 study, which primarily assesses safety in humans. Phase 1 studies are early tests, so while more information is needed, testing in humans suggests it is expected to be safe under controlled conditions.12345

Why are researchers excited about this trial's treatments?

Mosliciguat is unique because it is administered as a dry powder inhaler, offering a potentially more convenient and faster-acting delivery method compared to traditional pills or injections. This inhalation approach might provide quicker absorption, which could lead to faster therapeutic effects. Additionally, mosliciguat's novel mechanism of action involves targeting specific pathways in the body that current treatments might not address, potentially leading to better outcomes. Researchers are excited about this treatment because it could offer a new and effective option for patients, enhancing both convenience and efficacy.

What evidence suggests that mosliciguat could be effective?

This trial will compare two methods of administering mosliciguat to healthy subjects. Research suggests that mosliciguat might be particularly effective when inhaled. Studies in healthy men have shown that it remains in the body longer when inhaled than when taken orally or through an IV. This could improve outcomes for certain health issues. In other research, mosliciguat demonstrated positive effects in treating pulmonary hypertension, which is high blood pressure in the lungs. These early findings indicate potential benefits, but further research is needed to confirm its efficacy for specific conditions.15678

Who Is on the Research Team?

UM

Ubaldo Martin

Principal Investigator

Pulmovant, Inc.

Are You a Good Fit for This Trial?

This trial is for healthy adult males who are in good health as determined by medical exams, ECG, and lab tests. They must be willing to consent to the study. Men with recent respiratory infections, chronic lung diseases like COPD or asthma within the last 5 years, or conditions that could risk safety or study goals can't join.

Inclusion Criteria

Participants willing and able to provide informed consent
Considered to be in good health by the Investigator, as determined by medical history, physical examination, vital sign measurements, 12 lead electrocardiogram (ECG), and laboratory test results.

Exclusion Criteria

My recent respiratory infection symptoms cleared up at least 3 days ago.
I don't have any health issues or past surgeries that would risk my safety in the study.
I have had COPD, asthma, or another lung condition in the past 5 years.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive mosliciguat via dry powder inhaler and [14C]-mosliciguat orally and via IV to assess bioavailability, absorption, metabolism, and excretion

7 days
Daily visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessment of treatment-emergent adverse events

44 days

What Are the Treatments Tested in This Trial?

Interventions

  • Mosliciguat
Trial Overview The trial is testing mosliciguat's bioavailability when administered via a dry powder inhaler to healthy men. It's an open-label study where participants will know they're receiving mosliciguat and its absorption, metabolism, excretion will be studied over three periods.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Group I: Mosliciguat (RVT-2301)Experimental Treatment2 Interventions
Group II: 14C mosliciguatExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Pulmovant, Inc.

Lead Sponsor

Trials
1
Recruited
120+

Citations

A Phase 1 Study of Mosliciguat in Healthy, Adult MalesA way for patients with serious diseases or conditions who cannot participate in a clinical trial to gain access to a medical product that has ...
Results from Randomized Phase I Studies in Healthy MenThe results show that mosliciguat remains in the body for longer when given as an inhalation than when given orally or intravenously.
3.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/40402373/
Results from Randomized Phase I Studies in Healthy MenThe results show that mosliciguat remains in the body for longer when given as an inhalation than when given orally or intravenously.
A Study of Mosliciguat in PH-ILDThis is a Phase 2, randomized, double-blind, placebo-controlled, multi-center clinical study to evaluate the safety and efficacy of inhaled ...
Press Release, September 10, 2024Pulmovant presents positive proof-of-concept data from the Phase 1b ATMOS study of Mosliciguat in Pulmonary Hypertension at European Respiratory Society ...
Pharmacokinetics and Lung Deposition After ...Inhaled mosliciguat had a longer t max and half-life than oral mosliciguat. Accumulation data suggest formation of a mosliciguat depot in the lungs.
NCT06635850 | A Study of Mosliciguat in PH-ILDThis is a Phase 2, randomized, double-blind, placebo-controlled, multi-center clinical study to evaluate the safety and efficacy of inhaled mosliciguat in ...
Pulmovant Announces Publication of Pharmacokinetics ...Three Phase 1 studies support once-daily inhaled administration of mosliciguat with no evidence of serious systemic side effects.
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