A Multi-Center Study of Riociguat in Patients With Sickle Cell Diseases

Mark Gladwin130 enrolled

Overview

The proposed study is a Phase 2 multi-center, randomized, double-blind, placebo-controlled, parallel groups study aimed to evaluate the safety, tolerability and the efficacy of riociguat compared with placebo in patients with sickle cell disease (SCD).

This randomized study involves 12 weeks of treatment with riociguat pills or placebo pills, and a follow-up period of 30 days after treatment. The dose is adjusted every 2 weeks based on systolic blood pressure (SBP) and well-being assessed at that visit. Physical examinations, vital signs, blood tests and questionnaires will be performed at 2 week intervals during the double blinded study treatment. Echocardiogram, urine testing, six-minute walk distance and questionnaires will be assessed at the beginning and end of the treatment phase.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

130

Conditions

Sickle Cell Disease

Interventions

RiociguatDRUG

Riociguat 0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg and 2.5 mg three times a day for 12 weeks

PlaceboDRUG

Matching placebo to riociguat 0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg and 2.5 mg three times a day for 12 weeks

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age ≥ 18 years * Sickling disorder (HbSS, HbSC, HbSbeta-thalassemia, HbSD, HbSO-Arab documented by hemoglobin electrophoresis or HPLC fractionation) * At least one of the following findings: a. Systolic blood pressure ≥ 130 mm Hg on at least two occasions at least 1 day apart (one of these may be by history), b. Macroalbuminuria as manifested by urine albumin to creatinine ratio \> 300 mg/g, c. Tricuspid regurgitant velocity (TRV) \> 2.9 m/sec measured by echocardiography d. NT-proBNP level ≥ 160 pg/mL e. Urinalysis protein 1 + or higher. * Females of reproductive potential (FRP) must have a negative, pre-treatment pregnancy test. Post-menopausal women (defined as no menses for at least 1 year or post-surgical from bilateral oophorectomy) are not required to undergo a pregnancy test. * Females of reproductive potential must agree to use reliable contraception when sexually active. Adequate contraception is defined as any combination of at least 2 effective methods of birth control, of which at least one is a physical barrier (e.g. condoms with hormonal contraception or implants or combined oral contraceptives, certain intrauterine devices). Adequate contraception is required beginning at the signing of the informed consent form until one month after the last dose of riociguat. * Patients must be willing to provide a blood sample for DNA analysis. Exclusion Criteria: * Pregnant or breast feeding women * Patients with severe hepatic impairment defined as Child Pugh C * End stage renal disease requiring dialysis * Patients with eGFR \<30 mL/min/1.73m, where GFR is estimated based on CKD-epi equation * Patients on phosphodiesterase type 5 inhibitors (PDE-5) (such as sildenafil, tadalafil, vardenafil) and nonspecific PDE inhibitors (such as dipyridamole or theophylline) or nitrates * Patients on strong cytochrome P450 (CYP) and P-glycoprotein 1(P-gp)/BCRP inhibitors such as systemic azole antimycotics (eg: ketoconazole, itraconazole), or HIV protease inhibitors (such as ritonavir) * Patients on St. John's Wort * If patients are taking antihypertensive drugs, hydroxyurea, L-glutamine, crizanlizumab, or voxelotor prior to enrollment, they are excluded until the dose level is stable for at least three months * Systolic blood pressure \<95 mm Hg at Screening Visit 1 or 2 or Week 0 before randomization * Current enrollment in an investigational new drug trial. Patients are eligible for enrollment 30 days after the last dose of an investigational drug has been received * Evidence of qualitative urine drug test at screening for cocaine, phencyclidine (PCP), heroin, or amphetamines within three months prior to enrollment * Patients who have recently (last six months) experienced serious bleeding from the lung or have undergone a bronchial arterial embolization procedure. * Pulmonary hypertension associated with Idiopathic Interstitial Pneumonias * Medical disorder, condition, or history that in the investigator's judgment would impair the patient's ability to participate or complete this study or render the patient to be inappropriate for enrollment

Locations (20)

UCSF Benioff Children's Hospital Oakland

Oakland, California, United States

Outcomes

Primary Outcomes

Overall Incidence of Treatment Emergent Severe Adverse Events (SAE)

The primary endpoint was the proportion of participants who experienced at least 1 treatment-emergent serious adverse event (SAE), which was defined as any event occurring after the baseline visit (i.e., after initiation of study drug), adjudicated by a designated committee of protocol investigators and outside experts. SAEs were considered to be treatment-emergent if they started or worsened after the first dose of study medication and up to 7 days after end of study treatment.

Time frame: Baseline through 7 days after discontinuation of treatment, up to 13 Weeks

Secondary Outcomes

Frequency of SAE Due to Sickle Cell Related Painful Crisis

The proportion of participants with treatment-emergent SAE for sickle-cell related crises (Vaso-occlusive crises)

Time frame: Baseline through 7 days after discontinuation of treatment, up to 13 Weeks

Overall Incidences of Treatment-emergent Adverse Events (AEs)

Proportion of participants that experienced treatment-emergent AEs

Time frame: Baseline to Week 12

Incidences of Sickle Cell Related Clinical Complications

Incidence of Vaso-occlusive Crisis (VOC) between baseline and week 12

Time frame: Baseline to Week 12

Pain Intensity Using the Brief Pain Inventory

Brief Pain Inventory (BPI) short form - score ranges from 0 (no pain) to 10 (Pain as bad as you can imagine) Mean at 12 weeks assessed using ANCOVA adjusting for baseline.

Time frame: Baseline, 12 weeks

6-minute Walk Distance

6-minute walk distance was used to assess functional exercise capacity Mean at 12 weeks assessed using ANCOVA adjusting for baseline.

Data from ClinicalTrials.gov

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Howard University

Washington D.C., District of Columbia, United States

University of Miami

Miami, Florida, United States

Emory University School of Medicine

Atlanta, Georgia, United States

University of Illinois, Chicago

Chicago, Illinois, United States

Indiana University

Indianapolis, Indiana, United States

Tulane University

New Orleans, Louisiana, United States

Johns Hopkins University

Baltimore, Maryland, United States

Boston University Medical Center

Boston, Massachusetts, United States

New York Presbyterian Brooklyn Methodist Hospital

Brooklyn, New York, United States

...and 10 more locations

Time frame: Baseline, 12 weeks

Changes in the Dyspnea Borg Scale

Baseline to 12 weeks mean change of the Borg dyspnea scores, post 6MWT, using a linear regression model. Dyspnea Borg score was used to measure the level of severity of breathlessness perceived by the patient at the end of the 6MWD Test. The severity is measured on a 10-point scale with 0= nothing at all and 10=maximum severity of breathlessness.

Time frame: Baseline,12 Weeks

Fatigue Borg Scale

Fatigue Borg score was used to rank the participant's exertion at the end of the 6MWD Test. The rate of exertion was given according to a scale ranging from 0 (nothing at all) to 10=maximum severity of exertion Mean at 12 weeks assessed using ANCOVA adjusting for baseline.

Time frame: Baseline,12 weeks

Changes in Blood Pressure as the Main Pharmacodynamic (MAP)

Baseline to 12 weeks mean change of MAP, estimated with a repeated measures analysis (Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 10 weeks, 12 weeks) using a linear mixed model.

Time frame: Baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 10 weeks, 12 weeks

Tricuspid Regurgitant Velocity (TRV) Using Non-invasive Echocardiography

Mean TRV at 12 weeks assessed using ANCOVA, adjusting for baseline.

Time frame: Baseline, 12 Weeks

End-systolic Volume Using Non-invasive Echocardiography

Mean end-systolic volume (biplane) at 12 weeks, assessed using ANCOVA adjusting for baseline.

Time frame: Baseline,12 weeks

Ejection Fraction (Biplane) Using Non-invasive Echocardiography

Mean ejection fraction (biplane) at 12 weeks, assessed using ANCOVA adjusting for baseline.

Time frame: Baseline, 12 weeks

Changes in the Levels of Plasma NT-proBNP

Mean Change in the levels of plasma NT-proBNP from baseline to 12 weeks using a linear regression model.

Time frame: Baseline,12 weeks

Changes in Albumin/Creatinine Ratio

Albumin/Creatinine Ratio (ACR) mean change from baseline to 12 weeks using linear regression model.

Time frame: Baseline,12 weeks

Microalbuminuria

Odds ratio per week of microalbuminuria estimated with a repeated measures analysis (baseline, 12 weeks) using a generalized linear mixed model without random slope

Time frame: Baseline,12 weeks

Macroalbuminuria

Odds ratio per week of macroalbuminuria estimated with a repeated measures analysis (baseline, 12 weeks) using a generalized linear mixed model without random slope.

Time frame: Baseline,12 weeks

Changes in Glomerular Filtration Rate

Mean change in GFR to 12 weeks, estimated with a repeated measures analysis (Baseline, 4 weeks, 8 weeks, 12 weeks) a using a linear mixed model.

Time frame: Baseline, 4 weeks, 8 weeks, 12 weeks

Chronic Kidney Disease (CKD) Stage - Low Risk Versus at Least Moderately Increased Risk

Odds ratio (OR) per week of low-risk CKD stage versus at least moderately increased risk (includes moderately increased risk CKD, high increased risk CKD, and very high increased risk CKD) estimated with a repeated measures analysis (baseline, 12 weeks) using a generalized linear mixed model without random slope

Time frame: Baseline,12 weeks

Changes in Hemoglobin

Mean change in hemoglobin to 12 weeks, estimated with a repeated measures analysis (Baseline, 4 weeks, 8 weeks, 12 weeks) a using a linear mixed model.

Time frame: Baseline, 4 weeks, 8 weeks,12 weeks

Changes in Reticulocyte Count

Mean change in reticulocyte count to 12 weeks, estimated with a repeated measures analysis (Baseline, 4 weeks, 8 weeks, 12 weeks) a using a linear mixed model.

Time frame: Baseline, 4 weeks, 8 weeks,12 weeks

Changes in White Blood Cell Count

Mean change in White Blood Cell count to 12 weeks estimated with a repeated measures analysis (Baseline, 4 weeks, 8 weeks, 12 weeks) a using a linear mixed model.

Time frame: Baseline, 4 weeks, 8 weeks,12 weeks

Changes in Lactate Dehydrogenase (LDH)

Mean change in LDH to 12 weeks estimated with a repeated measures analysis (Baseline, 4 weeks, 8 weeks, 12 weeks) a using a linear mixed model.

Time frame: Baseline, 4 weeks, 8 weeks,12 weeks

Changes in Fetal Hemoglobin

Mean change in fetal hemoglobin from baseline to 12 weeks using a linear mixed model

Time frame: Baseline,12 weeks