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Ali Ataya, MD : Research

Critical Care Medicine Specialist, Pulmonologist (Lung Specialist)

Photo of Ali Ataya

Research at a glance

Top areas of exploration

  • Dyspnea , 15 publications
  • Lung Diseases , 7 publications
  • Hypertension, Pulmonary , 7 publications
  • Pulmonary Alveolar Proteinosis , 6 publications

Research activity

118 publications

396 citations

Why is this important?

Active clinical trials

IMPALA-2

160 subjects with autoimmune pulmonary alveolar proteinosis (aPAP) will be randomized to receive once daily treatment with inhaled molgramostim or placebo for 48 weeks. Subjects completing the 48 week placebo-controlled period will receive…

Investigator
Ali Ataya
Status
Accepting Candidates
Ages
18 Years - N/A
Sexes
All
ROR-PH-303 (APD811-303)

Study ROR-PH-303, ADVANCE EXTENSION, is an open-label extension (OLE) study for participants with WHO Group 1 PAH who have participated in another Phase 2 or Phase 3 study of ralinepag.

Investigator
Ali Ataya
Status
Accepting Candidates
Ages
18 Years - N/A
Sexes
All
United therapeutics 301

Study ROR-PH-301, ADVANCE OUTCOMES, is designed to assess the efficacy and safety of ralinepag when added to pulmonary arterial hypertension (PAH) standard of care or PAH-specific background therapy in subjects with World ÍøºìºÚÁÏ Organization (WHO)…

Investigator
Ali Ataya
Status
Accepting Candidates
Ages
18 Years - N/A
Sexes
All

My publications

118 publications

2025

A patient journey map for people living with autoimmune pulmonary alveolar proteinosis.

Respiratory medicine

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2025

Case report: Novel homozygous ACVRL1 missense variant in a family with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension: findings suggest a hypomorphic allele.

Frontiers in genetics

•

2025

Concurrent limited cutaneous systemic sclerosis and hereditary haemorrhagic telangiectasia.

The Lancet. Haematology

•

2025

Development of New Intrapulmonary Shunts in Pulmonary Arterial Hypertension Treated with Sotatercept.

American journal of respiratory and critical care medicine

2025

Glycogen storage disease type V: delayed diagnosis of a cause of exercise intolerance in a patient with hereditary haemorrhagic telangiectasia.

BMJ case reports

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