A Dose Titration Study to Assess the Effects of SAR407899 in Patients With MVA and/or Persistent Stable Angina Despite Angiographically Successful PCI

NCT ID: NCT03236311

Last Updated: 2022-03-24

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-12
• Study Completion Date: 2018-07-23

Brief Summary

Primary Objective:

To assess the effects of SAR407899 on coronary vasomotor function using the coronary flow reserve (CFR) in participants with microvascular angina (MVA) and/or persistent stable angina despite angiographically successful percutaneous coronary intervention (PCI).

Secondary Objectives:

• To assess the effects of SAR407899 on quality of life using Seattle Angina Questionnaire physical limitation scale (SAQ-PL) in participants with MVA and/or persistent stable angina despite angiographically successful PCI.
• To assess the safety of SAR407899 in participants with MVA and/or persistent stable angina despite angiographically successful PCI with a focus on identified risks such as hypotension and orthostatic hypotension.
• To assess SAR407899 plasma concentrations in MVA participants and/or persistent stable angina despite angiographically successful PCI.

Detailed Description

The total duration of study per participant was:

• up to 9 weeks for participants with previous coronary artery angiography or coronary computed tomography angiography (CCTA) within 24 months prior to screening with up to 4 weeks screening period, 3 weeks titration phase, 1 week maintenance period, and 1 week follow-up after the last investigational medicinal product administration.

or

• up to 11 weeks for participants with previous coronary artery angiography or CCTA between 24 months and 5 years prior to screening who need CCTA during screening period with up to 6 weeks screening period, 3 weeks titration phase, 1 week maintenance period, and 1 week follow-up after the last investigational medicinal product administration.

Conditions

Microvascular Coronary Artery Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

Matching placebo for 4 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Pharmaceutical form: Capsule Route of administration: Oral

Adenosine

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Regadenoson

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

13N-ammonia

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

82Rubidium

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

SAR407899

SAR407899 with dose titration over 4 weeks administration (3 week titration phase + 1 week maintenance phase).

Group Type: EXPERIMENTAL

SAR407899

Intervention Type: DRUG

Pharmaceutical form: Capsule Route of administration: Oral

Adenosine

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Regadenoson

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

13N-ammonia

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

82Rubidium

Intervention Type: DRUG

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Interventions

SAR407899

Pharmaceutical form: Capsule Route of administration: Oral

Intervention Type: DRUG

Placebo

Pharmaceutical form: Capsule Route of administration: Oral

Intervention Type: DRUG

Adenosine

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Intervention Type: DRUG

Regadenoson

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Intervention Type: DRUG

13N-ammonia

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Intervention Type: DRUG

82Rubidium

Pharmaceutical form: Solution for injection Route of administration: Intravenous

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female participants not at childbearing potential >=18 year-old or legal age of majority.
• Female participant if she has undergone sterilization at least 3 months earlier or was post-menopausal.
• Post-menopausal status was defined by having no menses for 12 months without an alternative medical cause.
• In females not treated with hormonal replacement therapy (HRT), menopausal status was confirmed by a high follicle stimulating hormone (FSH) level greater than 40 international units per litre (IU/L).
• In females on HRT and whose menopausal status was in doubt (i.e. in women aged less than 45 years), a highly effective contraception methods was required. Contraception was used during the whole study and for at least seven days corresponding to time needed to eliminate study treatment.
• Symptomatic stable angina pectoris (typical or atypical symptoms with an average of at least bi-weekly episodes over the past month).
• Participants with non-obstructive (<50% stenosis) coronary arteries or intermediate stenosis (between 50 and 70%) should have fractional flow reserve (FFR) >0.80 or instantaneous wave-free ratio (iFR) >0.89 on angiogram, documented within the previous 24 months*. In participants with stenting, a minimum diameter stenosis of <10% is required.

or Coronary computed tomography angiography (CCTA) with finding of non-obstructive coronary arteries within the past 24 months* in participants without previous percutaneous coronary intervention (PCI).

*Note: in cases of clinically suspected progression of atherosclerosis as per the Investigator, a more contemporary (i.e., 6 months) evidence should be provided.

or CCTA performed during screening period, with finding of non-obstructive coronary arteries, in participants diagnosed with microvascular angina (MVA) and stable angina without previous PCI who did not have a coronary angiogram or CCTA in the previous 24 months but between 24 months to 5 years.

• Baseline global coronary flow reserve (CFR) (measured during the study) assessed by 13N-ammonia or 82Rubidium positron emission tomography (PET) scan <2.0.

Exclusion Criteria

• Any use of nitrates (except short-acting nitrates) and/or dipyridamole and/or phosphodiesterase type 5 (PDE 5) inhibitors within one week prior to baseline PET scan or anticipated to be used during the study.
• Esophageal dysmotility or esophagitis.
• Participants with acute coronary syndrome (ACS) (myocardial infarction [MI] and/or unstable angina) in previous 3 months.
• Unsuccessful or incomplete coronary revascularization with residual obstructive stenosis or coronary artery disease (CAD) progression in native vessels as documented on invasive coronary angiography (>=50% stenosis) within 24 months of enrollment.
• Percutaneous coronary intervention performed at the time of an ACS (MI or unstable angina) in the previous 12 months.
• Recent PCI within the past 3 months.
• Participants with history of coronary artery bypass grafting (CABG).
• Recent (<=3 months) major surgery (i.e. valvular surgery, surgery for congenital heart disease), stroke, transient ischemic attack [TIA], sustained ventricular arrhythmia, clinically significant structural heart disease (moderate-severe valvular disease, hypertrophic cardiomyopathy, congenital heart disease, pulmonary hypertension).
• Regional local flow abnormal perfusion defects at baseline PET scan*.

*Note: if contemporary evidence with invasive coronary angiography or CCTA demonstrates non-obstructive coronary arteries or if the regional local flow abnormal perfusion defect on PET scan is consistent with previous studies then participant qualifies for the study.

• Participants with cardiac conduction abnormalities (second or third degree atrioventricular [AV] block, sick sinus syndrome, symptomatic bradycardia, sinus node disease) except in participants fitted with a functioning pacemaker.
• History or known carotid stenosis:
• Carotid stenosis (>50%) or
• History of carotid stenosis in participants with previous symptoms.
• Contraindication or known hypersensitivity to adenosine or regadenoson.
• Contraindication to aminophylline.
• Contraindication to vasodilator stress PET scan and/or CCTA if CCTA needed during screening.
• Inability to discontinue treatment with methylxanthines treatment within 24 hours prior to PET scan.
• Participant unable to read, understand and fill a questionnaire without any help (eg, partially visually impaired or blind).
• Systolic blood pressure (SBP) <110 millimeter of mercury (mmHg) at baseline.
• Presence at baseline of symptomatic orthostatic hypotension (SBP decrease of 20 mmHg or more at Minute 3 or Minute 5 between seated and standing position), or asymptomatic orthostatic hypotension with a decrease in SBP equal or greater than 30 mmHg at Minute 3 or Minute 5 when changing from the seated to the standing position.
• Renal impairment with estimated glomerular filtration rate (eGFR) <50 milliliter/minute/1.73 square meter (mL/min/1.73 m^2) at screening and baseline.
• Drug-induced liver injury related criteria:
• Underlying hepatobiliary disease.
• Alanine Aminotransferase (ALT) >3 times the upper limit of normal (ULN).

The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Sciences & Operations

Role: STUDY_DIRECTOR

Sanofi

Locations

Investigational Site Number 8400003

Los Angeles, California, United States

Investigational Site Number 8400001

Jacksonville, Florida, United States

Investigational Site Number 8400013

Wellington, Florida, United States

Investigational Site Number 8400008

Baltimore, Maryland, United States

Investigational Site Number 8400006

Boston, Massachusetts, United States

Investigational Site Number 8400010

Philadelphia, Pennsylvania, United States

Investigational Site Number 2080001

København NV, , Denmark

Investigational Site Number 5280001

Nijmegen, , Netherlands

Investigational Site Number 4100002

Seoul, , South Korea

Investigational Site Number 7520001

Lund, , Sweden

Countries

United States; Denmark; Netherlands; South Korea; Sweden

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

2016-000629-38

Identifier Type: -

Identifier Source: secondary_id

U1111-1182-1709

Identifier Type: OTHER

Identifier Source: secondary_id

ACT14656

Identifier Type: -

Identifier Source: org_study_id