Full Press Release Details
Therapeutics Announces Initiation of IMPAHCT Phase 2b/Phase 3 Trial of AV-101 In Pulmonary Arterial Hypertension
Mass. - December 15, 2021 - Aerovate Therapeutics, Inc. (Nasdaq: AVTE), a clinical-stage biopharmaceutical company
focused on developing drugs that meaningfully improve the lives of patients with rare cardiopulmonary diseases, today announced the initiation
of its Inhaled Imatinib Pulmonary Arterial Hypertension Clinical Trial (IMPAHCT) Phase
2b/Phase 3 trial to evaluate the safety and efficacy of AV-101 (dry powder inhaled imatinib) in adult patients with Pulmonary Arterial
is a real need for new treatment options for PAH patients that work differently from our currently approved therapies," said Dr.
Nicholas Hill, Chief, Pulmonary, Critical Care and Sleep Division, Tufts Medical Center and Chair of the IMPAHCT clinical advisory board.
"Imatinib has shown promise as a therapy for PAH and if AV-101 can deliver improvements for patients with fewer of
the systemic adverse events associated with oral imatinib in PAH, it could represent a real advancement for patients."
are excited and humbled to initiate this Phase 2b/Phase 3 trial of AV-101," said Tim Noyes, Chief Executive Officer at Aerovate.
"Starting enrollment represents an important milestone for Aerovate Therapeutics and advances our goal of improving the lives of
patients suffering from rare cardiovascular diseases."
expects to report top-line results from the Phase 2b portion of IMPAHCT in mid-2023.
information about this trial is available at
is a multi-national, placebo-controlled Phase 2b/Phase 3 trial in adults with pulmonary arterial hypertension (PAH) that will continuously
enroll patients as the study progresses from Phase 2b to Phase 3. The Phase 2b portion of the trial will evaluate three doses
of AV-101 compared to placebo to identify an optimal dose based on the primary endpoint, change in pulmonary vascular resistance (PVR)
over 24 weeks versus placebo, and safety, tolerability, and other clinical measures. The Phase 3 portion of the trial will compare patients
taking the optimal dose selected in Phase 2b of AV-101 with placebo. The primary endpoint of the Phase 3 portion of the trial will be
change in 6-minute walk distance (6MWD) over 24 weeks versus placebo.
Pulmonary Arterial Hypertension (PAH)
arterial hypertension (PAH) is a rare, progressive disease characterized by cellular hyperproliferation of the pulmonary vasculature
that affects approximately 70,000 people in the United States and Europe. The disease process involves remodeling, constriction and occlusion
of the small pulmonary arteries resulting in elevated blood pressure in the pulmonary circulation. PAH can cause strain on the heart,
leading to limitation of physical activity, heart failure and reduced life expectancy. Existing vasodilator drugs fail to treat the underlying
cellular proliferation causing the disease.
is a proprietary dry powder inhaled formulation of the anti-proliferative drug imatinib. Dosed specifically for PAH, AV-101 is designed
for delivery by an easy-to-use dry powder inhaler, directly into the lungs to maximize potential clinical benefit and limit systemic
adverse effects. In a recent Phase 1 clinical trial, AV-101 was generally well-tolerated by healthy adult volunteers with no serious
adverse events associated with AV-101.
Aerovate Therapeutics, Inc.
is a clinical stage biopharmaceutical company focused on developing drugs that meaningfully improve the lives of patients with rare cardiopulmonary
diseases. Aerovate's initial focus is on advancing AV-101, its dry powder inhaled formulation of the drug imatinib for the treatment
Note Regarding Forward-Looking Statements
press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended.
Forward-looking statements can be identified by words such as "anticipate," "believe," "continue,"
"could," "estimate," "expect," "future," "goal," "intend," "look
forward to," "may," "plan," "potential," "predict," "project," "potential,"
seek," "strategy," "should," "target," "will," "would" and similar
expressions regarding future periods. These forward-looking statements include, but are not limited to, statements regarding the therapeutic
potential of AV-101; our expectations regarding patient enrollment for the Phase 2b portion of our Phase 2b/Phase 3 trial of AV-101
in PAH; our business plans and objectives for AV-101, including expectations regarding timing and success of the our Phase 2b/Phase
3 clinical trial, including the timing of top-line results, the therapeutic potential and clinical benefits of AV-101 and potential
regulatory submissions and approvals for AV-101; and our growth and goals as a company.
forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to
a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed
or implied by any forward-looking statements contained in this press release, including, without limitation, those risks and uncertainties
related to the therapeutic potential of AV-101, and the timing associated with patient recruitment, initiation and continuation of our
Phase 2b/Phase 3 trial of AV-101 in PAH patients and timing of top-line results, the impact of the COVID-19 pandemic on our business,
clinical trials, operations and goals, positive results from a clinical study may not necessarily be predictive of the results of future
or ongoing clinical studies, regulatory developments in the United States and foreign countries, and other risks identified in our filings
with the Securities and Exchange Commission ("SEC"), including our Registration Statement on Form S-1, and subsequent filings
with the SEC. We caution you not to place undue reliance on any forward-looking statements, which speak only as of the date they are
made. We disclaim any obligation to publicly update or revise any such statements to reflect any change in expectations or in events,
conditions or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ
from those set forth in the forward-looking statements. Any forward-looking statements contained in this press release represent our
views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date.