Trial | NCT03217331  Report issue

Official Title

CRD-102 for Right Heart Failure in Patients With Left Ventricular Assist Devices

  • Phase

    Phase 1/Phase 2

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    6
This is a Phase 1b/IIa, single centre, non-randomised open-label uncontrolled study to assess safety, effect and PK of oral CRD-102 in patients with RHF associated with the presence of an LVAD.
The study will be conducted over a 40 day time period inclusive of screening and follow up time periods. Eligible subjects will receive oral CRD-102 for 14 days.
Study Started
Mar 06
2018
Primary Completion
Oct 10
2018
Study Completion
May 30
2019
Last Update
Jun 25
2019

Drug CRD-102

14 mg CRD-102 capsules administered twice daily orally for 14 days.

CRD-102 Treatment Experimental

CRD102 Treatment

Criteria 

Inclusion Criteria:

Patients are enrolled only if they met the following criteria.

Males and females aged 18-85 years inclusive
Have received a LVAD (HeartWare HVAD, HeartMate II) at least 30 days prior to screening.

Stable LVAD patients with evidence of ongoing right heart failure as evidenced by raised right atrial pressure indicated by JVP >6cm OR measured right atrial pressure ≥12mmHg within the 3 months prior to or at Baseline OR dilated IVC on echocardiography PLUS all of the following;

ongoing diuretic therapy;
echocardiography in the 3 months prior to or at Baseline showing at least mild impairment in overall RV systolic function by visual assessment together with a TAPSE < 14mm.
Able to give written informed consent and agree to adhere to all protocol requirements.
All patients will be required to have an implanted cardiaoverter defibrillator. (ICD)

Exclusion Criteria:

Hemodynamically unstable patients.
Hypotension (MAP<60 or systolic BP <90 mmHg) at Screening or Baseline
Hypertension (MAP>95 or systolic BP >130 mmHg) at Screening or Baseline
Ventricular tachycardia or ventricular fibrillation in the past 30 days or poorly controlled atrial fibrillation (ventricular rate >120 bpm)
Concurrent participation in another investigational device study or prior participation in which a device was implanted and remains in place
Receipt of any investigational research agent within 30 days or 5 half-lives (whichever is longer) prior to Baseline.
Current treatment with intravenous inotropes or levosimendan, or treatment within the 2 weeks prior to Screening
Significant renal (eGFR<25 ml/min/1.73 sq m) or hepatic (bilirubin >3mg/dL) impairment or anemia (Hb <90g/dL) at Screening or Baseline.
Expected heart transplantation within the study period.
Pregnancy
History of allergic reaction to milrinone or any excipients in the study drug.
No Results Posted