New heart failure drug shows promise in hospitalized patients
NCT ID NCT06815471
First seen Jun 27, 2026 · Last updated Jul 23, 2026 · Updated 2 times
Summary
This study tests an investigational drug called COR-1167 in 300 people hospitalized with worsening heart failure. Participants receive either the drug or a placebo for 28 days. Researchers measure how well the body removes fluid, changes in weight, heart function, and symptoms. The goal is to see if COR-1167 can improve recovery and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- COR-1167
- What this could lead to
- If successful, this could lead to a new treatment option for people hospitalized with worsening heart failure, helping them recover faster and feel better.
- What could go wrong
- This is an early Phase 2 trial with only 300 participants, so results may not apply to all heart failure patients. The drug may not work better than standard care or could have side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2025
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 85 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed written informed consent * Heart failure hospitalization (HFH) during previous 12 months * Prescribed an oral loop diuretic for at least 1 month preceding the index event * NT-proBNP ≥1,000 pg/mL or BNP ≥250 pg/mL * Requires treatment with i.v. diuretics for volume overload * At least 1 risk factor for diuretic resistance * Admitted to the hospital not more than 48 hours prior to randomization Exclusion Criteria: * Index event primarily triggered by an acute event (e.g. AMI, PE, arrhythmia) * Requirement for i.v. inotropic therapy or i.v. vasodilators, mechanical ventilation, high-flow oxygen therapy, or NIV * Requirement for, or planned use of LVADs, IABP, or any type of MCS * History of solid organ transplant or active on a transplant list * SBP \<100 mmHg * eGFR \< 20 mL/min/1.73 m2 * CABG, PCI, implantation of CRT, heart valve procedure or any cardiac surgery within 1 month prior to screening or planned during the study * Severe stenotic cardiac valvular disease * Severe chronic pulmonary disease requiring chronic steroid therapy or chronic oxygen therapy (\> 2 L/min) * Uncorrected severe hyperthyroidism or hypothyroidism * Severe restrictive, obstructive, or infiltrative cardiomyopathy * Body weight \< 70 kg * Use of any investigational drug(s) within 5 half-lives of screening * At high risk of death (defined as life expectancy ≤1 year) from causes other than heart failure or any disease that, in the opinion of the Investigator, will preclude their safe participation in this study, and will make implementation of the protocol or interpretation of the study results difficult * Presence of any other conditions (e.g. geographic, social) actual or anticipated, that the Investigator feels would restrict or limit the subject's participation or compliance with all study procedures Subject is the Investigator or any Subinvestigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the study
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Worsening heart failure are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
55 sites in 8 countries. The list below names each one and where it is.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Acad. G. Chapidze Emergency Cardiology Center LTD, Department of Internal Medicine and Medical Research
Tbilisi, 0159, Georgia
-
Acad. G.Chapidze Emergency Cardiology Center, LTD, Department of Multi-center Clinical Trials
Tbilisi, 0159, Georgia
-
Aleksandre Aladashvili Clinic LLC
Tbilisi, 0102, Georgia
-
Bokhua Memorial Cardiovascular Center LTD
Tbilisi, 0159, Georgia
-
Budapesti Uzsoki Utcai Kórház, Kardiológia Osztály
Budapest, 1145, Hungary
-
Clinical Hospital Center "Dr Dragisa Misovic Dedinje"
Belgrade, 11000, Serbia
-
Cone Health Moses Cone Hospital
Greensboro, North Carolina, 27401, United States
-
Consorcio Hospital General Universitario de Valencia
Valencia, 46014, Spain
-
Craiova County Emergency Clinical Hospital
Craiova, 200642, Romania
-
Emergency County Clinical Hospital Arad, Cardiology department
Arad, 310037, Romania
-
Fakultní nemocnice Brno
Brno, 62500, Czechia
-
Fakultní nemocnice Ostrava
Ostrava, 70852, Czechia
-
General Hospital Leskovac, Cardiology Department
Leskovac, 16000, Serbia
-
Georgian Dutch Hospital
Tbilisi, 0167, Georgia
-
Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar, Murcia, 30120, Spain
-
Hospital Clínico Universitario de Valencia
Valencia, Valencia, 46010, Spain
-
Hospital Universitari i Politecnic La Fe
Valencia, 46026, Spain
-
Hospital Universitario Hospital Virgen del Rocío
Seville, 41013, Spain
-
Hospital Universitario Puerta de Hierro Majadahonda
Majadahonda, Madrid, 28222, Spain
-
Hospital Universitario Ramon y Cajal
Fuencarral-El Pardo, Madrid, 28034, Spain
-
I Klinika Kardiologii, Uniwersyteckie Centrum Kliniczne
Gdansk, 80-214, Poland
-
II Klinika Kardiologii, SPZOZ Centralny Szpital Kliniczny Uniwersytetu Medycznego w Lodzi
Lodz, 92-213, Poland
-
Indiana University Health Methodist Hospital
Indianapolis, Indiana, 46202, United States
-
Institute For Treatment and Rehabilitation "Niska Banja"
Niška Banja, 18205, Serbia
-
Institute for Cardiovascular Diseases Dedinje
Belgrade, 11000, Serbia
-
Institutul de Urgenta pentru Boli Cardiovasculare "Prof. Dr. C.C. Iliescu", Cardiologie 1
Bucharest, 022328, Romania
-
Institutul de Urgenta pentru Boli Cardiovasculare "Prof. Dr. C.C. Iliescu", Cardiologie 3
Bucharest, 022328, Romania
-
Instytut Chorób Serca, Zakład Badań Klinicznych Chorób Układu Krążenia, Uniwersytecki Szpital Kliniczny im. Jana Mikulicza-Radeckiego we Wrocławiu
Wroclaw, 50-556, Poland
-
Kliniczny Szpital Wojewódzki nr 2 im. Św. Jadwigi Królowej w Rzeszowie
Rzeszów, 35-301, Poland
-
Klinika Kardiologii i Chorób Wewnętrznych z Oddziałem Intensywnego Nadzoru Kardiologicznego (OINK), Uniwersytecki Szpital Kliniczny w Białymstoku
Bialystok, 15-276, Poland
-
LTD "Israeli-Georgian Medical Research Clinic Healthycore"
Tbilisi, 0112, Georgia
-
LTD Tbilisi Heart Center
Tbilisi, 0186, Georgia
-
NC Heart and Vascular Research, LLC
Raleigh, North Carolina, 27607, United States
-
Nemocnice Slaný
Slaný, 27401, Czechia
-
Oddział Kliniczny Kardiologii i Intensywnej Terapii Kardiologicznej
Torun, 87-100, Poland
-
Ohio State University
Columbus, Ohio, 43210, United States
-
Pécsi Tudományegyetem, Klinikai Központ, I. sz. Belgyógyászati Klinika
Pécs, 7624, Hungary
-
SP ZOZ Szpital Uniwersytecki w Krakowie
Krakow, 30-688, Poland
-
Sdružené zdravotnické zařízení Krnov
Krnov, 79401, Czechia
-
Semmelweis Egyetem, Általános Orvostudományi Kar, Városmajori Szív- és Érgyógyászati Klinika
Budapest, 1122, Hungary
-
South Oklahoma Heart Research, LLC
Oklahoma City, Oklahoma, 73135, United States
-
Spitalul Clinic Colentina
Bucharest, 20125, Romania
-
Spitalul Clinic Municipal de Urgenta Timisoara
Timișoara, 300079, Romania
-
St. Michael's Hospital LLC
Tbilisi, 0159, Georgia
-
Szegedi Tudományegyetem, Általános Orvostudományi Kar, Családorvosi Intézet
Szeged, 7625, Hungary
-
Tbilisi Heart and Vascular Clinic, LTD
Tbilisi, 0159, Georgia
-
University Clinical Center Kragujevac, Clinic for Cardiology
Kragujevac, 34000, Serbia
-
University Clinical Center Nis, Clinic for Cardiology
Niš, 18000, Serbia
-
University Clinical Center of Serbia, Clinic for Cardiology, Department for the testing and treatment of congenital and acquired heart defects
Belgrade, 11000, Serbia
-
University Clinical Center of Serbia, Clinic for Cardiology, Emergency Cardiology Department
Belgrade, 11000, Serbia
-
University Clinical Center of Serbia, Clinic for Cardiology, Heart Failure Ward
Belgrade, 11000, Serbia
-
Wayne State University - Detroit Receiving Hospital
Detroit, Michigan, 48201, United States
-
Wayne State University - Sinai Grace Hospital
Detroit, Michigan, 48235, United States
-
Zala Vármegyei Szent Rafael Kórház, Kardiológiai Osztály
Zalaegerszeg, 8900, Hungary
-
Zespół Opieki Zdrowotnej w Klodzku, Oddzial Kardiologii
Kłodzko, 57-300, Poland
More trials for these conditions
Other studies related to the condition(s) this trial covers.