AMBLE: Efficacy and Safety Study of Ambrisentan in Chinese Patients With Pulmonary Arterial Hypertension

Sponsor

RenJi Hospital (Other)

Overall Status

Completed

CT.gov ID

NCT05437224

Collaborator

Shanghai Zhongshan Hospital (Other), The First Affiliated Hospital with Nanjing Medical University (Other), Shanghai Pulmonary Hospital, Shanghai, China (Other), Xinqiao Hospital of Chongqing (Other), The Affiliated Hospital of Qingdao University (Other), First Affiliated Hospital of Chongqing Medical University (Other), Wuhan Asia Heart Hospital (Other)

Enrollment

Location

Arm

37.7

Actual Duration (Months)

2.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This multicenter, open label, single-arm study is aim at investigating the the efficacy and safety of china made ambrisentan in Chinese subjects with PAH.

Condition or Disease	Intervention/Treatment	Phase
Pulmonary Arterial Hypertension	Drug: Ambrisentan	Phase 3

Detailed Description

Pulmonary arterial hypertension is a hemodynamic and pathophysiological state, which can cause progressive hyperplasia of pulmonary vascular walls and elevated pulmonary arterial pressure for various reasons. Ambrisentan is a selective endothelin-A (ETA) receptor antagonist with vasodilatory, antiproliferative and vascular remodeling effects at a dose of 5 mg or 10 mg once daily, oral. A number of international clinical studies have shown that ambrisentan can improve the hemodynamic parameters, WHO functional classification and exercise tolerance of PAH patients, and improve the survival rate. The domestic Ambrisentan tablet is produced by Jiangsu Hansoh Pharmaceutical Group Co., Ltd. under the trade name of "Pu Nuo An". It has been developed and completed according to the consistency evaluation standard after the bioequivalence test, and is currently listed in mainland China. In view of the low price of the domestic ambrisentan, in order to verify its efficacy and safety in the real world, this post-marketing multicenter clinical study was carried out.

Study Design

Study Type:

Interventional

Actual Enrollment :

80 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Multicenter Open Label Study to Evaluate Efficacy and Safety of China Made Ambrisentan in Chinese Patients With Pulmonary Arterial Hypertension

Actual Study Start Date :

Dec 18, 2018

Actual Primary Completion Date :

Jan 9, 2022

Actual Study Completion Date :

Feb 6, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: ambrisentan Open Label	Drug: Ambrisentan eligible subjects received 5 mg ambrisentan orally once daily for a 12-week primary evaluation period. Subjects then proceeded to a 12-week dose adjustment period during which dose titration to 10 mg was allowed.

Arm

Intervention/Treatment

Experimental: ambrisentan

Open Label

Drug: Ambrisentan

eligible subjects received 5 mg ambrisentan orally once daily for a 12-week primary evaluation period. Subjects then proceeded to a 12-week dose adjustment period during which dose titration to 10 mg was allowed.

Outcome Measures

Primary Outcome Measures

Change From Baseline to 12 weeks and 24weeks in 6-minute Walk Distance [Baseline, week 12 and week 24]
The 6-minute walk test (6MWT) is a non-encouraged test, performed in a 30 m long flat corridor, where the patient is instructed to walk as far as possible, back and forth around two cones, with the permission to slow down, rest, or stop if needed. These guidelines were provided to all sites. For patients who had never performed a 6MWT previously, a training test was required before the qualifying tests for inclusion were performed.

Secondary Outcome Measures

Time to Clinical Worsening of Pulmonary Arterial Hypertension (PAH) up to Week 24, Assessed as the First Occurrence of a Clinical Worsening Events [From Baseline to week 24]
Clinical Worsening Events included a 15% decrease from baseline on the 6-minute walk test, hospitalization for pulmonary hypertension complications, dosing or escalation of pulmonary hypertension-targeted drugs, atrial septostomy, lung transplantation, or death. Time to clinical worsening of PAH is the time from baseline to the first clinical occurrence of a Clinical Worsening Events.
Change from baseline to week 12 and 24 in Borg Dyspnea Index (BDI) sores [Baseline, week 12 and week 24]
The BDI was calculated by using a 10-point scale (0 = None, 10 = Maximum).
Number of participants with a change from baseline to week 12 and 24 in WHO functional class [Baseline, week 12 and week 24]
The WHO FC was determined by the investigator as follows: Class I - Participants with pulmonary hypertension (PH) but without resulting limitation of physical activity; II- Participants with PH resulting in slight limitation of physical activity; III - Participants with PH resulting in marked limitation of physical activity; IV - Participants with PH with inability to carry out any physical activity without symptoms.
Changes from baseline to week 12 and 24 in BNP plasma levels [Baseline, week 12 and week 24]
BNP is a surrogate maker of heart failure.
Number and severity of Participants With Any Adverse Events [From Baseline to week 24]
An adverse event is defined as any adverse medical event in a patient that is not necessarily causally related to treatment. An adverse event can thus be any adverse or non-therapeutic sign (including abnormal laboratory results), symptom or disease temporally related to the use of the drug product, whether or not considered drug-related.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 75 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Age ≥18 years old and ≤75 years old, regardless of gender;
patients weighing ≥ 40 kg;
Patients diagnosed with PAH in Group 1 of the WHO Updated Clinical Classification of Pulmonary Hypertension (WHO functional class II or III);
6 min walk test (6MWT), walking distance ≥ 50 m;
Right heart catheterization performed within 6 months prior to screening and meeting the following hemodynamic criteria:

mean pulmonary artery pressure ≥ 25 mm Hg；
Pulmonary vascular resistance ≥ 240 dyn·s·cm-5;
Pulmonary artery wedge pressure or left ventricular end-diastolic pressure ≤ 15 mmHg;

Subject receiving calcium channel blocker (CCB) drugs, only those whose doses have been stabilized for more than 4 weeks at the time of screening are allowed to be included in the study;
Pulmonary function testing performed within 6 months prior to screening and meeting the following criteria：

Total lung capacity ≥ 60% of normal predicted value;
Forced expiratory volume in one second (FEV1) ≥ 55% of normal expected value;

Female subjects of childbearing potential must have a negative pregnancy test at the Screening Visit and Day 0;
Females subjects of childbearing potential must use a medically acceptable method of contraception (eg, hormone therapy, IUD, barrier methods such as condoms or cervical caps) during the study;
Sign written informed consent

Exclusion Criteria:

Patients diagnosed with WHO updated PH clinical classification of group 2, 3, 4, 5;
Endothelin receptor antagonist therapy (eg, bosentan) has been discontinued prior to enrollment due to safety or tolerability concerns (non-drug-induced liver function abnormalities);
Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels > 2 times ULN;
Serum bilirubin level > 1.5 times ULN;
severe hepatic insufficiency (Child-Pugh class C);
severe renal insufficiency (creatinine clearance <30 mL/min);
Hemoglobin concentration < 10 g/dL or hematocrit < 30%;
Contraindications to treatment identified by laboratory tests, physical examination, medical history, or other investigations
severe hypotension (diastolic < 50 mm Hg or systolic < 90 mm Hg);
Clinically significant aortic or mitral valve disease, pericardial constriction, restrictive or congestive cardiomyopathy, fatal arrhythmias, LV ejection fraction < 45%, LV outflow tract obstruction, symptomatic coronary heart disease, spontaneously low blood pressure;
A history of malignancy within 5 years prior to enrollment, except for basal cell carcinoma of the skin and carcinoma in situ of the cervix;
Subject taking endothelin receptor antagonists such as ambrisentan, bosentan and macitentan within 4 weeks prior to enrollment;
pregnant and lactating women;
Subject deemed unsuitable for participation in this study by other investigators