PHIRST-1: Tadalafil in the Treatment of Pulmonary Arterial Hypertension

Phase 3

Completed

• Conditions: Pulmonary Hypertension
• Interventions: Drug: placebo; Drug: tadalafil

• Registration Number: NCT00125918
• Lead Sponsor: Eli Lilly and Company

Brief Summary

The purpose of this study is to evaluate the safety and effectiveness of tadalafil for the treatment of pulmonary arterial hypertension.

Detailed Description

This is a randomized, double-blind, placebo-controlled, multicenter study. The key measure of effectiveness of the study drug will be determined using a 6-minute walk test. Eligible patients will be treated for 16 weeks and may be eligible to enter a 52-week extension phase study (PHIRST-2). Study procedures for both studies (PHIRST-1 and PHIRST-2) will include routine blood tests, medical history, physical exams, questionnaire responses, and exercise tests.

Study Timeline

• Study Start: 2005-08
• Study First Submitted: 2005-08-01
• Study First Submitted QC: 2005-08-01
• Study First Posted: 2005-08-02
• Primary Completion: 2007-08
• Study Completion: 2007-08
• Status Verified: 2008-02
• Last Update Submitted: 2008-02-13
• Last Update Posted: 2008-02-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 406

Inclusion Criteria

• At least 12 years of age.
• Body weight at least 40 kg (approximately 88 pounds).
• Pulmonary hypertension (PAH) that is either idiopathic; related to collagen vascular disease; related to anorexigen use; associated with an atrial septal defect (resting SaO2 greater than or equal to 88%); with surgical repair, of at least 1 year duration, of a congenital systemic-to-pulmonary shunt.
• If on bosentan, must be at the maximal dose of 125 mg twice daily for a minimum of 12 weeks prior to screening and have an AST/ALT less than 3 times normal.
• History of PAH established by a resting mean pulmonary artery pressure greater than or equal to 25 mm Hg, pulmonary artery wedge pressure less than or equal to 15 mm Hg, and pulmonary vascular resistance greater than or equal to 3 Wood units via right heart catheterization
• Have World Health Organization functional class I, II, III or IV status.
• Have a qualifying 6-minute walk test distance at screening
• Have no evidence of significant parenchymal lung disease

Exclusion Criteria

• Are nursing or pregnant.
• PAH due to conditions other than noted in the above inclusion criteria.
• History of left-sided heart disease.
• History of atrial septostomy within 3 months before study entry
• History of angina pectoris or other condition that was treated with long-or short-acting nitrates within 12 weeks before administration of study drug.
• History of symptomatic coronary disease.
• Have any therapy with a prostacyclin or analogue, L-arginine, phosphodiesterase (PDE) inhibitor, or investigational drug within 4 weeks before administration of study drug.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	placebo	Placebo
2	tadalafil	2.5 mg tadalafil
3	tadalafil	10 mg tadalafil
5	tadalafil	40 mg tadalafil
4	tadalafil	20 mg tadalafil

Primary Outcome Measures

Name	Time	Method
6 minute walk distance change from baseline to Week 16	16 weeks

Secondary Outcome Measures

Name	Time	Method
World Health Organization (WHO) functional class, Borg dyspnea, cardiopulmonary hemodynamics, quality of life - change from baseline to Week 16	16 weeks
Time to first occurrence of clinical worsening	Not defined

Trial Locations

Locations (1)

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.; 🇮🇹 Bergamo, Italy