Purpose

This 2-part study will evaluate PHIN-214 given as a single one-time dose (Part 1) and in multiple doses (given as daily doses for 28-days) (in Part 2). Specifically, this study evaluates PHIN-214, to determine the safety, tolerability, and pharmacokinetic effects of PHIN-214, and to establish the maximum tolerated dose or optimal beneficial dose in patients with Child Pugh A and B Cirrhosis.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 75 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. History of cirrhosis based on histology or a combination of clinical, radiological, or biochemical assessment and classified as Child-Pugh A or B 2. Participants may be male or female aged 18 to 75 years. 3. Body mass index (BMI) within the range 18 to 40 kg/m2 (inclusive) at screening. 4. Female participants must be non-pregnant, non-lactating, or of non-childbearing potential or using highly efficient contraception for the full duration of the study

Exclusion Criteria

  1. Significant abnormalities in medical history or on physical examination, including: respiratory disease requiring therapy or history of respiratory failure, cardiovascular disease or hypertension, electrocardiogram abnormalities or history of significant EKG abnormalities. 2. History of diabetes insipidus, syndrome of inappropriate antidiuretic hormone secretion, or any other disorder associated with fluid or sodium imbalance. 3. Significant kidney disease 4. Hepatic encephalopathy (HE) or altered mental status requiring hospitalization; variceal bleeding or upper gastrointestinal bleeding; or type 1 hepatorenal syndrome with acute kidney injury (HRS-AKI) during the previous 3 months prior to Screening. 5. Acute-on-chronic liver failure. 6. Recipient of a patent transjugular intrahepatic portosystemic shunt (TIPS). 7. Known positive HIV serology confirmed by HIV viral load. 8. Subjects with acute infections, including acute viral hepatitis (subjects with chronic hepatitis B are eligible if treatment regimen is stable ≥ 3 months prior to study inclusion).

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Sequential Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
single dose of PHIN-214
Participants in Part 1 will receive one dose of PHIN-214 administered subcutaneously. Dose level will be assigned in ascending doses to observe initial safety and tolerability. A Safety Committee will review information from each patient and determine the dose level for the subsequent participants.
  • Drug: PHIN-214 Subcutaneous injection
    subcutaneous injection(s) with PHIN-214 terlipressin derivative
    Other names:
    • Terlipressin derivative
Experimental
multiple daily dosing of PHIN-214
Participants in Part 2 will be trained to give themselves a daily dose of PHIN-214 at home by subcutaneous injection for 28-days. The dose level assigned to each participant will be determined by a Safety Committee after reviewing information from the last participants' experience and compilation of experiences on all previous participants. Dose level advancement will be guided throughout the study by the experiences and information collected from each participant.
  • Drug: PHIN-214 Subcutaneous injection
    subcutaneous injection(s) with PHIN-214 terlipressin derivative
    Other names:
    • Terlipressin derivative

Recruiting Locations

Arizona Liver Health
Chandler, Arizona 85224
Contact:
Angie Coste, FNP-C
480-470-4000
acoste@azliver.com

Southern California Research Center
Coronado, California 92118
Contact:
Kasey Seyer
619-522-0330
kasey@researchscrc.com

Tandem Clinical Research
Marrero, Louisiana 70072
Contact:
Alexis Johnson
504-934-8424
AJohnson@tandemclinicalresearch.com

Mayo Clinic
Rochester, Minnesota 55905
Contact:
Amy Olofson, RN
507-538-6547
Olofson.Amy@mayo.edu

Cleveland Clinic
Cleveland, Ohio 44195
Contact:
Keralee Morey
216-215-0808
moreyk@ccf.org

University of Pennsylvania
Philadelphia, Pennsylvania 19104
Contact:
Margaret Bussineau
215-615-3755
Margaret.Bussineau@Pennmedicine.upenn.edu

Methodist Health System, Dallas Medical Center
Dallas, Texas 75203
Contact:
Crystee Cooper
214-947-1280
clinicalresearch@mhd.com

VA North Texas Healthcare System
Dallas, Texas 75216
Contact:
Jacqueline O'Leary, MD
214-857-0403
Jacqueline.Oleary@va.gov

Texas Liver Institute
San Antonio, Texas 78215
Contact:
Eric Lawitz, MD
210-253-3426
Lawitz@txliver.com

More Details

NCT ID
NCT05490888
Status
Recruiting
Sponsor
PharmaIN

Study Contact

Cynthia C Jones
206-568-1450
PHIN.214001@pharmain.com

Detailed Description

PHIN-214 action has similar actions as another medication called "terlipressin or TERLIVAZ®." Terlipressin has been shown to reduce portal hypertension, improve renal function, and induce natriuresis in cirrhotic patients with ascites without hepatorenal syndrome (HRS). It is approved in several countries including the US for the treatment of bleeding esophageal varices and HRS type 1 and is usually administered using multiple IV doses given by bolus injections in the hospital. This study is an open label, first in human study of PHIN-214. PHIN-214 is a terlipressin derivative administered subcutaneously. It is a partial V1a agonist which is designed to reduce splanchnic blood pooling and portal hypertension. A resultant increase in systemic pressure and renal arterial pressure may increase kidney perfusion and creatinine clearance. This study will evaluate a single dose of PHIN-214 (in Part 1) and in Part 2, daily doses of PHIN-214 for up to 28-days (called multiple ascending doses) of PHIN-214 to determine the safety, tolerability, pharmacokinetics and pharmacodynamics of PHIN-214 in subjects with advanced cirrhosis.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.