Serelaxin To Lower Portal Pressure (STOPP)

University of Edinburgh

Status and phase: Completed; Phase 2

Conditions: Hypertension, Portal; Liver Cirrhosis

Treatments: Drug: Placebo; Drug: Serelaxin

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02669875

STOPP

Details and patient eligibility

About

Portal hypertension (an increase in blood pressure in the portal vein that carries the blood from the intestine and spleen to the liver) underlies most of the serious complications of liver cirrhosis. This randomised placebo controlled study in people with liver cirrhosis evaluates the acute effects serelaxin (RLX030) infusion on portal hypertension and liver blood flow.

Full description

This study will investigate the effects of the investigational drug serelaxin (a recombinant form of the peptide human relaxin-2) on portal hypertension in patients with liver cirrhosis. The investigators will measure portal pressure by hepatic venous pressure gradient (HVPG) and hepatic blood flow by indocyanine green (ICG) clearance to evaluate the potential benefits of the drug. In a recently completed small exploratory open-label phase 2 study (EudraCT no. 201200023626, NCT01640964), Part B demonstrated that serelaxin can lower portal pressure.

Enrollment: 15 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female adult subjects over 18 years of age
2. Able to provide written informed consent and able to understand and willing to comply with the requirements of the study
3. Clinical imaging-diagnosed or biopsy-proven liver cirrhosis of any aetiology
4. Evidence of portal hypertension either on imaging or previous endoscopy
5. Patients with large/grade 3 varices as identified by endoscopy within 6 months of screening must be in an endoscopic band ligation programme at the time of study entry
6. Suspected hepatic venous pressure gradient (HVPG) ≥10 mmHg at baseline

Exclusion criteria

1. Pregnancy or breast feeding
2. Women of child-bearing potential not using highly effective methods of contraception
3. Severe liver failure defined by one of the following: Prothrombin activity <40%, Bilirubin >5 mg/dL (85umol/L), hepatic encephalopathy > grade I
4. A history of variceal bleed within 1 month prior to visit 1
5. Presence of any non-controlled and clinically significant disease that could affect the study outcome or that would place the patient at undue risk
6. Hepatocellular carcinoma or history of malignancy of any organ system (other than localized basal cell carcinoma of the skin) treated or untreated
7. Portal vein thrombosis
8. Previous surgical shunt or TIPSS
9. Current use of beta-blockers or nitrates, any other drug therapy known to have an influence on portal pressure (diuretics permitted provided patients have been on a stable dose for at least 30 days)
10. History of drug or alcohol abuse within 1 month of enrolment
11. Sitting Systolic Blood Pressure <110 mmHg at screening visit or within 10 minutes prior to starting study drug infusion
12. Use of other investigational drugs within 5 half-lives of enrolment, or within 30 days/until the expected pharmacodynamic effect has returned to baseline, whichever is longer
13. Significant arrhythmias, which include any of the following: sustained ventricular tachycardia, bradycardia with sustained ventricular rate < 45 beats per minute or atrial fibrillation/flutter with sustained ventricular response of > 90 beats per minute at rest, or Long QT syndrome or corrected QT interval (QTc) > 450 msec (QT correction will be performed using the Fridericia correction method: QTcF = QT/RR0.33) for males and > 460 msec for females at screening visit
14. Documented hypersensitivity to intravenous contrast agents and/or iodine
15. Severe renal impairment (eGFR<30mL/min /1.73m2)
16. Significant left ventricular outflow tract obstructions (e.g., severe valvular aortic stenosis, obstructive cardiomyopathy), severe mitral stenosis, restrictive amyloid myocardiopathy, acute myocarditis
17. Severe aortic insufficiency or severe mitral regurgitation for which surgical or percutaneous intervention is indicated
18. Major neurologic event including cerebrovascular events, within 30 days prior to screening
19. Clinical evidence of acute coronary syndrome currently or within 30 days prior to enrolment
20. History of hypersensitivity to study drug serelaxin or study drug ingredients
21. Inability to follow instructions or comply with follow-up procedures.
22. Permanent pacemaker, cardiac resynchronisation device or implantable cardioverter-defibrillator in situ

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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15 participants in 2 patient groups, including a placebo group

Serelaxin

Active Comparator group

Description:

IV infusion of serelaxin (RLX030) for 2 hours

Treatment:

Drug: Serelaxin

Placebo

Placebo Comparator group

Description:

IV infusion of placebo (20mM sodium acetate pH5) matched to serelaxin for 2 hours

Treatment:

Drug: Placebo