Emphower PoC: Empagliflozin in Pulmonary Arterial Hypertension
Study Details
Study Description
Brief Summary
The aim of the study is to determine whether conducting a randomized placebo-controlled clinical trial is feasible, safe for the patient and whether the treatment is well tolerated in patients with idiopathic pulmonary arterial hypertension.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
This is a prospective single-center, phase IIa, single arm, open label, interventional proof-of-concept study conducted in 8 patients with idiopathic pulmonary arterial hypertension receiving stable therapy. Patients will receive standard treatment plus 10 mg once daily empagliflozin oral tablets for 12 weeks. The primary endpoints of the study are safety, feasibility and tolerability of treatment with empagliflozin. This study should explore whether conducting a randomized double blind placebo controlled study with empagliflozin treatment is feasible, safe for the patient and well tolerated by study participants. The explore potential benefit of treatment with empagliflozin, subjects will receive an MRI and ultrasound of the heart, blood biomarkers will be assessed, a six minute walking test will be conducted and two questionnaires will be administered. During treatment, the hospital will be visited to closely monitor funcational class and the safety of the drug through blood and physical examination. Adverse events will be accurately registered.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Empagliflozin
|
Drug: Empagliflozin 10 MG
10 mg once daily empagliflozin oral tablets for 12 weeks
|
Outcome Measures
Primary Outcome Measures
- Tolerability: the number of patients who have to prematurely discontinue treatment due to intolerability or adverse events. [12 weeks]
- Feasibility: time needed to include all patients and number of patients needed to screen. [12 weeks]
- Safety: the number of adverse events (AEs), severe adverse events (SAEs), adverse event of special interest (AESI) and suspected unexpected serious adverse reactions (SUSARs). [12 weeks]
Secondary Outcome Measures
- Right ventricle ejection fraction (RVEF) measured using MRI [12 weeks]
RVEF is calculated using the RVESV, RVEDV
- Right ventricle mass measured using MRI [12 weeks]
- Left ventricle ejection fraction (LVEF) measured using MRI [12 weeks]
LVEF is calculated using the LVESV, LVEDV
- Stroke volume (SV) measured using MRI [12 weeks]
SV is calculated using the LVESV, LVEDV
- Tricuspid annular plane systolic excursion (TAPSE) measured using transthoracic ultrasound [12 weeks]
- Estimated sPAP measured using transthoracic ultrasound [12 weeks]
- Right ventricle fractional area change (RVFAC) measured using transthoracic ultrasound [12 weeks]
- Blood biomarkers [12 weeks]
Endpoints: Expression of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) and bone morphogenetic protein receptor II (BMPR2) in peripheral blood mononuclear cells (PMBC)
- Blood safety biomarkers [12 weeks]
Fasting glucose, N-terminal prohormone of Brain Natriuretic Peptide (NT-proBNP) and creatinine in blood.
- Urine safety biomarkers [12 weeks]
Ketones, nitrites, leukocytes and glucose in urine test strip (dipstick).
- Functional class [12 weeks]
World Health Organization Function Classification of Pulmonary Hypertension. Outcome: Class I, Class II, Class III or Class IV
- Six-Minute Walk Distance [12 weeks]
Six-minute walk distance (6MWD) will be measured by the 6-minute walk test (6MWT). The test should preferably be conducted on a straight 30 metre track. The patient is instructed to walk as far as possible for six minutes. One lap is demonstrated. The patient is told that slowing down can be necessary, and after pausing are encouraged to start walking as soon as possible.
- Quality of life measured with use of the EMPHASIS-10 questionnaire [12 weeks]
The emPHasis-10 is a short questionnaire for assessing Health-related quality of life in pulmonary arterial hypertension. The questionnaire comprises 10 items that are formatted as a semantic six-point differential scale and results in a score out of 50 where a higher score represents a higher symptom burden.
- Quality of life measured with use of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) questionnaire [12 weeks]
The CAMPHOR questionnaire contains 65 items in total. The measure consists of three different scales: a symptom scale assessing energy, breathlessness and mood (25-items; low score indicating minimal symptoms); activity limitations scale with a 3-point rating system (15-items; range 0 to 30, lower score indicating minimal activity limitation); and a QoL scale (25-items; lower score indicating better QoL). It is negatively weighted; a higher score indicates worse QoL and greater functional limitation.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age ≥ 18 years
-
Diagnosis of idiopathic PAH
-
Documented diagnostic right heart catheterization (RHC) at any time prior to screening confirming diagnosis of WHO diagnostic pulmonary hypertension Group I: PAH with subtype idiopathic PAH. The documented RHC shows all of the following criteria:
-
mPAP > 20 mmHg at rest
-
Pulmonary artery wedge pressure (PAWP) or left ventricular end-diastolic pressure (LVEDP) ≤ 15 mmHg at rest
-
PVR ≥ 240 dyn·sec/cm5 (3 Wood units) at rest
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Symptomatic pulmonary hypertension classified as World Health Organization (WHO) functional class (FC) II, III or IV
-
PAH therapy is at stable (per investigator) dose levels of standard of care (SoC) therapies for at least 90 days prior screening. SoC therapy refers to a therapy consisting of at least 1 agent from a list including: an endothelin-receptor antagonist (ERA), a phosphodiesterase 5 (PDE5) inhibitor, a soluble guanylate cyclase stimulator, and/or a prostacyclin analogue or receptor agonist (SC/inhaled/PO).
Exclusion Criteria:
-
Any subject who received any investigational medication within 1 month prior to the start of this study or who is scheduled to receive another investigational drug during the course of this study. Patients participating in a purely observational trial will not be excluded
-
Females of childbearing potential, defined as a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy or 2) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 months), unable or unwillingly to either:
-
Use highly effective methods of birth control according to the International Conference on harmonisation of pharmaceuticals for human use (ICH) that result in a low failure rate of less than 1% per year when used consistently and correctly
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Highly effective methods include hormonal contraception (for example, birth control pills, injection, implant, transdermal patch, vaginal ring); intrauterine device (IUD); tubal ligation (having your tubes tied); or a partner with a vasectomy who has completed follow-up to confirm a successful procedure
-
Have a negative pregnancy tests as verified by the investigator prior to starting study therapy and agrees to have an extra pregnancy test 8 weeks after start of the study
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Contraindication for CMR imaging as defined in the protocol of the Amsterdam UMC "Kwaliteitsdocument Cardiale MRI (Versie 1)". The list of contra-indications includes: claustrophobia, ferromagnetic implants, implanted cardioverter defibrillator (ICD) or pacemaker (except for the MR conditional) and ball-in-cage mechanic heart valve.
-
Impaired renal function, defined as eGFR < 30 mL/min/1.73 m2 (CKD-EPI) or requiring dialysis
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History of chronic severe (Child Pugh classification score >10, Appendix 1) or active liver disease defined as serums transaminases >5 x upper limit of normal (ULN) or bilirubin > 1.5 x ULN
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History of ketoacidosis
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Known allergy, intolerance or hypersensitivity to empagliflozin or other SGLT-2 inhibitors
-
Use of lithium compounds and being unable or unwillingly to increase the monitoring frequency of lithium levels
-
Current or scheduled use of the following Uridine glucuronosyltransferase (UGT) inducers: phenytoin, rifampicin, carbamazepine, lamotrigine, ritonavir, efavirenz, tipranavir, phenobarbital, testosterone propionate and nelfinavir.
-
Current or prior use of a SGLT-2 inhibitor
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Heart transplant recipient or listed for heart transplant
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Chronic pulmonary disease requiring home oxygen or steroid maintenance therapy
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Symptomatic hypotension and/or a systolic blood pressure (SBP) < 90 mmHg at screening
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Gastrointestinal (GI) surgery or GI disorder that could interfere with absorption of trial medication in the investigator's opinion
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Presence of any other disease than pulmonary arterial hypertension with a life expectancy of <1 year in the investigator's opinion
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Women who are pregnant, nursing, or who plan to become pregnant while in the trial
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History of severe (previously required or prolonged patient hospitalization, resulted in persistent or marked disability/incapacity) or recurrent (≥2 infections in six months or ≥3 infections in one year) genital infections.
-
History of severe hypoglycaemia (<40 - 30 mg/dL = <2.2 - 1.7 mmol/L), previous hospitalisation for hypoglycaemia or seizures attributed to hypoglycaemia
-
Active solid or haematological malignancy, with the exception of fully excised or treated basal cell carcinoma, cervical carcinoma in-situ, or ≤ 2 squamous cell carcinomas of the skin
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History or suspicion of inability to cooperate adequately
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Any condition that, in the investigator's opinion, makes them an unreliable trial subject or unlikely to complete the trial
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Amsterdam UMC, location VUmc
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 81866
- 2022-002400-20
- 2022-501512-33-00