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Recruiting Phase 1/2 NCT06638502

Safety of HRX215 in Patients After Minor and Major Liver Resection

Phase 1/2 – combined early trial
Conditions: Liver Resection Colorectal Carcinoma Liver Metastases

Sponsor: HepaRegeniX GmbH

trial.available_in: БГ
Overview
The goal of this clinical trial is to learn if HRX215 is safe, tolerable and active in adults who have undergone liver resection due to colorectal carcinoma metastases. The objectives are: 1. to learn about the safety and tolerability of HRX215 2. to learn about how the body absorbs, distributes, and gets rid of HRX215. 3. to learn about clinical activity of HRX215 Researchers will compare HRX215 to a placebo (a look-alike substance that contains no drug) to investigate safety, tolerability and clinical activity in participants taking HRX215.
Description
The study is designed to evaluate primarily the safety of HRX215, first after minor liver resection and subsequently in participants after major liver resection. Participants undergoing major liver resection will start treatment shortly before liver resection surgery and will receive 28 days of treatment with HRX215 or placebo twice daily with follow up visits at 3 and 6 months. Participants will take HRX215 or a placebo twice a day for 28 days. Daily visits for the first 7 days of treatment for checkups and tests which may either be in the hospital or outpatient after 3 days. Clinic visits every two weeks for the next two visits. Additional clinic visits 3 months and 6 months after the start of treatment. The pharmacokinetics will be compared with the results of the phase I studies in healthy subjects. Secondary objectives will include evaluation of liver volume and liver volume increase postoperatively.
Who can participate
Inclusion Criteria: * Participants with liver metastases originating from colon carcinoma planned for R0-intended hepatectomy for colorectal liver metastases * Part 1 only: stable participants within 1-3 days after minor liver resection, normal non-tumor liver parenchyma * Part 2 and 3 only: Major liver resection. * Low estimated risk for post-hepatectomy liver failure PHLF Further inclusion criteria apply Exclusion Criteria: * Liver Cirrhosis * Preoperative presence of clinical ascites * Any other hepatobiliary cancer * BMI \>35 kg/m2 * ASA Score \>4 * Peritoneal carcinomatosis Further exclusion criteria apply
Interventions
HRX215 capsules
DRUG
Placebo capsules
DRUG
Locations 4
Israel (3)
Rabin Medical Center
Petah Tikva
NOT_YET_RECRUITING
Eran Sadot, MD, PhD, Professor
Sheba Medical Center
Ramat Gan
NOT_YET_RECRUITING
Tel-Aviv Sourasky MC
Tel Aviv
NOT_YET_RECRUITING
Nir Lubezky, MD, PhD, Professor
United States (1)
Mayo Clinic
Rochester , Minnesota
Technical details
Status
Recruiting
Phase
Phase 1/2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
75 Years
Healthy volunteers
No
Start date
06.05.2025
Completion date
31.12.2027
Registry ID
NCT06638502
Source
clinicaltrials.gov
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