TPIP-202 (NCT05147805) was a phase 2b, randomised, placebo-controlled, 16-week trial in patients with WHO Group 1 PAH who were receiving up to 2 other background therapies. Following screening, participants were randomised 2:1 to either TPIP capsules once daily (80-640 µg, with a 3-week up-titration) or a matching placebo. The primary endpoint was the change from baseline in pulmonary vascular resistance at week 16. In total, 102 participants were randomised.
Prof. Ekkehard Grünig (University of Heidelberg, Germany) presented the results. The study met its primary endpoint, with a least-squares mean ratio of pulmonary vascular resistance of 0.63 at week 16 for TPIP versus 0.97 for placebo (adjusted ratio 0.65; 95% CI 0.54-0.79; P<0.001). Additionally, TPIP demonstrated a 35.5 m improvement in the 6-minute walk distance compared to the placebo after 16 weeks of treatment (95% CI 11.23-60.73; P=0.003). In total, 5.8% of participants discontinued TPIP, but none discontinued placebo. Adverse events were more common with TPIP, including cough (40.6% vs 21.2%, mostly mild events), headache (31.9% vs 15.2%), and fatigue (10.1% vs 3.0%) [1].
“The study showed a positive effect on the primary endpoint, with a 35% reduction in pulmonary vascular resistance alongside improvement in 6-minute walk distance,” concluded Prof. Grünig. “The drug was well-tolerated, and this success supports initiation of a phase 3 program, planned for next year.”
- Grünig E, et al. A randomized, double-blind, placebo-controlled study of treprostinil palmitil inhalation powder (TPIP) in patients with pulmonary arterial hypertension (PAH). ERS Congress, 27 September–1 October 2025, Amsterdam, the Netherlands.
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Table of Contents: ERS 2025
Featured articles
Early data suggest a potential benefit of taladegib in idiopathic pulmonary fibrosis
Astegolimab shows promise as a potential treatment for chronic obstructive pulmonary disease
Pulmonary Hypertension
TPIP-202 results confirm the efficacy of treprostinil palmitil inhalation powder in pulmonary arterial hypertension
Sotatercept is becoming a treatment option for patients with newly diagnosed pulmonary arterial hypertension
Lung Cancer and Other Clinical Insights
Does paracetamol cause eczema or bronchiolitis in infants?
Morphine is not effective for chronic breathlessness and raises safety concerns
How accurate are large language models for spirometry interpretation?
Durvalumab in combination with chemotherapy shows promise for patients with SCLC and poor performance status
Obstructive Airway Diseases
Dupilumab is superior to omalizumab in adults with chronic rhinosinusitis with nasal polyps and asthma
Budesonide/glycopyrronium/formoterol fumarate dihydrate for inadequately controlled asthma
Budesonide-formoterol reliever outperforms salbutamol in children with mild asthma
Astegolimab shows promise as a potential treatment for chronic obstructive pulmonary disease
Mepolizumab preserves lung function for up to 2 years in eosinophilic COPD
Respiratory Infections and Inflammation
Are patients with pulmonary sarcoidosis overtreated with corticosteroids?
Are mucoactive agents helpful in patients with bronchiectasis?
Brensocatib is efficacious in patients with bronchiectasis and more than 2 annual exacerbations
Inhaled heparin improves outcomes in non-intubated COVID-19 patients
Can children with infectious conditions requiring oxygen therapy be discharged at a SpO2 of 88%?
Beta-lactam antibiotics plus doxycycline are an alternative to azithromycin in severe community-acquired pneumonia
Interstitial and Fibrotic Lung Diseases
Updated results from FIBRONEER-IPF confirm nerandomilast efficacy over 76 weeks
Early data suggest a potential benefit of taladegib in idiopathic pulmonary fibrosis
TETON-2 highlights inhaled treprostinil as a treatment option for idiopathic pulmonary fibrosis
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