A Dose Escalation Study to Evaluate the Effect of RT234 in Subjects With Pulmonary Arterial Hypertension

Pulmonary Arterial Hypertension Clinical Trial

Official title:

A Phase 2a, Dose Escalation Study to Evaluate the Effect of RT234 on Cardiopulmonary Hemodynamics in Subjects With Pulmonary Arterial Hypertension

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05343637
• Other study ID #: RT234-CL201
• Secondary ID: ACTRN12619001178
• Status: Completed
• Phase: Phase 2
• Start date: July 30, 2019
• Est. completion date: January 17, 2020

Study information

• Verified date: April 2022
• Source: Respira Therapeutics, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This multicenter, open label, Phase 2a study is designed to evaluate the effect of inhaled RT234 delivered in a dose escalation manner on the change in pulmonary vascular resistance (PVR) in subjects with Pulmonary Arterial Hypertension (PAH) undergoing Right heart catheterization (RHC).

This study is also known as Vardenafil Inhaled for Pulmonary Arterial Hypertension PRN Phase 2a (VIPAH-PRN 2a) study

Description:

The drawbacks of current therapies and the lack of an approved as needed (PRN) treatment for PAH that improves exercise ability and quality of life, form the basis for development of RT234 (inhaled vardenafil). The current study will identify the effective dose(s) of RT234 to acutely improve pulmonary vascular hemodynamics when delivered in a dose escalation manner in subjects with World Health Organization (WHO) Group 1 PAH undergoing RHC. In addition, this study will also provide valuable efficacy and safety insights into the interactions between RT234 and background disease-specific PAH therapy on pulmonary hemodynamics and right heart function.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 14
• Est. completion date: January 17, 2020
• Est. primary completion date: January 17, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Between 18 and 80 years of age, inclusive.

2. Diagnosis of RHC-confirmed WHO Group 1 PAH in any of the following three categories:

Idiopathic, primary or familial pulmonary arterial hypertension (IPAH, PPH, or FPAH); OR PAH associated with one of the following connective tissue diseases (CTD):

1. Systemic sclerosis (scleroderma)

2. Limited scleroderma

3. Mixed connective tissue disease

4. Systemic lupus erythematosus

5. Overlap syndrome

6. Other autoimmune disorders;

OR PAH associated with:

1. Human immunodeficiency virus (HIV) infection with no evidence of opportunistic infection in the preceding 6 months;

2. Simple, congenital systemic-to-pulmonary shunts at least one-year post-surgical repair.

3. Exposure to legal drugs, chemicals and toxins, such as fenfluramine, derivatives, other anorexigens, toxic rapeseed oil or L-tryptophan. Subjects with PAH associated with illegal drug use, such as methamphetamine, were excluded.

3. Previous diagnosis with PAH with the following conditions:

1. Stable PAH without significant adjustments of disease-specific background PAH therapy, at least 3 months prior to RHC procedure;

2. If on corticosteroids, has been receiving a stable dose of = 20 mg/day of prednisone (or equivalent dose of other corticosteroid) for at least 30 days prior to RHC procedure.

4. Pulmonary Function Tests within 24 months prior to RHC procedure that fulfilled the following criteria (pulmonary function; (PFT may be assessed at Screening if historical PFT results are not available):

1. Forced Expiratory volume in one second (FEV1) = 60% predicted (pre-bronchodilators);

2. FEV1/ forced expiratory vital capacity (FVC) = 60% (pre-bronchodilators);

3. FVC = 60% predicted.

Exclusion Criteria:

1. Baseline systemic hypotension, defined as MAP < 50 mmHg or systolic blood pressure (SBP)< 90 mmHg at Screening.

2. Requirement of intravenous inotropes within 30 days prior to RHC procedure.

3. Use of oral, topical or inhaled nitrates within 14 days prior to RHC procedure.

4. Uncontrolled systemic hypertension: SBP > 160 mmHg or diastolic blood pressure (DBP) >100 mmHg at Screening.

5. History of portal hypertension or chronic liver disease, including active viral replication of hepatitis B and/or hepatitis C or classified as having moderate to severe hepatic impairment (Child-Pugh Class B-C).

6. Chronic renal insufficiency as defined by serum creatinine > 2.5 mg/dL at Screening or requires dialysis.

7. History of atrial septostomy.

8. Unrepaired congenital heart disease (CHD).

9. Pericardial constriction; restrictive or congestive cardiomyopathy.

10. History of left ventricular ejection fraction (EF) < 40% by multiple gated acquisition scan (MUGA), angiography, echocardiography, or cardiac magnetic resonance imaging (CMRI).

11. Symptomatic coronary disease with demonstrable ischemia.

12. Poorly controlled asthma defined by active wheezing and/or cough at the time of Screening or day of participation in Parts A and B.

13. Clinically significant intercurrent illness (including lower respiratory tract infection) or clinically significant surgery within 30 days prior to study drug administration.

14. Clinical RHC < 14 days prior to Screening.

15. History of non-arteritic anterior ischemic optic neuropathy (NAION) or retinitis pigmentosa.

Related Conditions & MeSH terms

• Familial Primary Pulmonary Hypertension
• Hypertension
• Pulmonary Arterial Hypertension

Intervention

Combination Product:
• Drug: RT234 - vardenafil inhalation powder; Device: RS01 dry powder inhaler (RS01 DPI)
RT234 is a drug/device combination product composed of vardenafil hydrochloride as the drug constituent and will utilize RS01 DPI device.

Locations

Country	Name	City	State
Australia	St Vincent's Hospital	Darlinghurst	New South Wales
Australia	Royal Hobart Hospital	Hobart	Tasmania
Australia	The Alfred Hospital	Melbourne	Victoria

Sponsors (1)

Lead Sponsor	Collaborator
Respira Therapeutics, Inc.

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluation of adverse events (AEs)	Evaluation of AEs will be measured by clinical examination and participant self-reporting. Known or possible adverse events include headache, lightheadedness and cough.	Screening to Day 30
Primary	Peak plasma concentration (Cmax)	Change in Cmax at each dose level on Day 1.	At baseline, 5, 15, 30, 45 and 60 minutes post-end of inhalation for the first RT234 dose and at 5, 15, 30, 45, 60, 75, 90, 105 and 120 minutes post-end of inhalation for the second RT234 dose.
Primary	Time to peak plasma concentration (Tmax)	Change in Tmax at each dose level on Day 1.	At baseline, 5, 15, 30, 45 and 60 minutes post-end of inhalation for the first RT234 dose and at 5, 15, 30, 45, 60, 75, 90, 105 and 120 minutes post-end of inhalation for the second RT234 dose.
Primary	Area under the plasma concentration versus time curve (AUC)	Change in AUC at each dose level on Day 1.	At baseline, 5, 15, 30, 45 and 60 minutes post-end of inhalation for the first RT234 dose and at 5, 15, 30, 45, 60, 75, 90, 105 and 120 minutes post-end of inhalation for the second RT234 dose.
Primary	Terminal half-life	Change in terminal half-life at each dose level on Day 1.	At baseline, 5, 15, 30, 45 and 60 minutes post-end of inhalation for the first RT234 dose and at 5, 15, 30, 45, 60, 75, 90, 105 and 120 minutes post-end of inhalation for the second RT234 dose.
Primary	Change in pulmonary vascular resistance (PVR)	Maximal change from baseline in PVR assessed at the time by right heart catheterisation (RHC).	At baseline, 5, 15, 30, 45 and 60 minutes post-end of inhalation for the first RT234 dose and at 5, 15, 30, 45, 60, 75, 90, 105 and 120 minutes post-end of inhalation for the second RT234 dose on Day 1.