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NCT05548296PHASE2Recruiting

A Phase 2 Study of ACR-368 in Endometrial Adenocarcinoma

Acrivon Therapeutics

Start Date

8/29/2022

Completion Date

11/30/2027

Summary

This is an open label Phase 2 study to evaluate the efficacy and safety of ACR-368 as monotherapy or with ultra-low dose gemcitabine (ULDG) sensitization in participants with endometrial cancer.

Detailed Description

OncoSignature Selected Cohorts (Arms 1 and 2): Participants in Arms 1 \& 2 will be allocated into two arms based on prospectively predicted sensitivity to ACR-368 using the OncoSignature® Companion Diagnostic test, as follows: Arm 1: OncoSignature Positive tumors Arm 2: OncoSignature Negative tumors (completed) OncoSignature Unselected Cohort (Arm 3 \& Arm 4): In Arm 3 and Arm 4, participants will not require a biopsy or OncoSignature result. Participants in Arm 1 and Arm 4 will receive ACR-368 as monotherapy. Participants in Arms 2 and 3 will receive ACR-368 with ULDG sensitization. Participants in all arms will be treated until disease progression, unacceptable toxicity or any criterion for stopping the study drug or withdrawal from the trial occurs. Arms 1 and 2 do not apply to sites in the European Union (EU), which will enroll subjects in Arm 3 and Arm 4.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: General 1. Participant must be able to give signed, written informed consent. 2. Participant must have histologically documented, high-grade endometrial cancer. Arms 1 and 2 1. All high-grade epithelial endometrial histological subtypes are eligible including: endometrioid (all Grade 3), serous, carcinosarcomas, clear-cell carcinoma, and mixed histologies. Note: Subjects with p53 mutant Grade 2 endometrioid cancer are eligible Arms 3 and 4 2. Serous carcinoma or mixed tumors with a majority component of serous carcinoma or carcinosarcoma where the carcinomatous component is serous carcinoma. 3. Treatment History Requirements: Arms 1 and 2 1. Subject must have received prior platinum-based chemotherapy 2. Subject must have received prior anti-PD-(L)1 therapy 3. Subject must not have received more than three lines of prior systemic therapy Arms 3 and 4 <!-- --> 1. Subject must have received prior platinum-based chemotherapy 2. Subject must have received prior anti-PD-(L)1 therapy 3. Subject must not have received more than two lines of prior systemic therapy 4. Participant must have histologically confirmed metastatic cancer that has progressed during or after at least 1 prior therapeutic regimen. 5. Participant must have at least 1 measurable lesion per RECIST v1.1 criteria (by local Investigator) in a baseline tumor imaging that has been obtained within 28 days of the treatment start. Participant must have radiographic evidence of disease progression based on RECIST v1.1 criteria following the most recent line of treatment. 6. Arm 1 and 2 only: Participant must be willing to provide tissue from a newly obtained tumor biopsy from an accessible tumor lesion not previously irradiated after written informed consent. Newly obtained is defined as a specimen taken after written informed consent is obtained, during the 28-day Screening period. Note: Subjects at EU sites are not eligible for Arm 1 and Arm 2 7. For all subjects participating in Arm 3 and 4, archival tumor tissue must be provided either during or after screening either as a tissue block or at least 20 unstained slides. 8. Participant must have stabilized or recovered (Grade 1 or baseline) from all prior therapy related toxicities, except as follows: 1. Alopecia is accepted. 2. Endocrine events from prior immunotherapy stabilized at ≤ Grade 2 due to need for replacement therapy are accepted (including hypothyroidism, diabetes mellitus, or adrenal insufficiency). 3. Neuropathy events from prior cytotoxic therapies stabilized at ≤ Grade 2 are accepted. 9. Participant must have an Eastern Cooperative Oncology Group Performance Status 0 or 1. 10. Participant must have an estimated life expectancy of longer than 3 months in the clinical judgment of the investigator. 11. Participant must have adequate organ function at Screening, defined as: 1. Absolute neutrophil count \> 1500 cells/µL without growth factor support within 2 weeks prior to obtaining the hematology values at Screening. 2. Hemoglobin ≥ 9.0 g/dL. 3. Platelets ≥ 150,000 cells/µL without transfusion within 1 week prior to obtaining the hematology values at Screening. 4. Renal function is defined as Glomerular filtration rate (GFR) ≥ 50 mL/min/1.73m2. Note: GFR may be estimated using site standard methods (e.g., CKD-EPI, MDRD, or Cockcroft-Gault) or measured using 24-hour urine collection or Chrome-EDTA clearance, as per site standard practice. 5. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × upper limit of normal (ULN); ≤ 5 × ULN if liver metastases are present. 6. Total bilirubin ≤ 1.5 × ULN not associated with Gilbert's syndrome. If associated with Gilbert's syndrome ≤ 3 x ULN is acceptable. 7. Serum albumin ≥ 3 g/dL. 12. Participant must have adequate coagulation profile as defined below if not on anticoagulation. If subject is receiving anticoagulation therapy, then subject must be on a stable dose of anticoagulation for ≥ 1 month: 1. Prothrombin time within 1.5 x ULN. 2. Activated partial thromboplastin time within 1.5 x ULN. Exclusion Criteria: General 1. Participant with known symptomatic brain metastases requiring \> 10 mg/day of prednisolone (or its equivalent). Participants with previously diagnosed brain metastases are eligible if they have completed their treatment, have recovered from the acute effects of radiation therapy or surgery prior to the start of ACR-368 treatment, fulfill the steroid requirement for these metastases, and are neurologically stable based on central nervous system imaging ≥ 4 weeks after treatment. 2. Participant has mesenchymal tumors of the uterus. 3. Participant has a history of clinically meaningful ascites, defined as history of paracentesis or thoracentesis with therapeutic intent, within 4 weeks of Screening. Subjects with planned therapeutic paracentesis or thoracentesis between Screening and Cycle 1 Day 1 dosing are excluded. 4. Participant had systemic therapy or radiation therapy within 3 weeks prior to the first dose of study drug. 5. Participants has known human immunodeficiency virus (HIV), hepatitis B, or hepatitis C infection that is considered uncontrolled based on the criteria included in Appendix 2. 6. Participant has a history of clinically meaningful coagulopathy, bleeding diathesis. 7. Participant has cardiovascular disease, defined as: 1. Uncontrolled hypertension defined as blood pressure \> 160/90 mmHg at Screening confirmed by repeat (medication permitted). 2. History of torsades de pointes, significant Screening electrocardiogram (ECG) abnormalities, including ventricular rhythm disturbances, unstable cardiac arrhythmia requiring medication, pathologic symptomatic bradycardia, left bundle branch block, second degree atrioventricular (AV) block type II, third degree AV block, Grade ≥ 2 bradycardia, uncorrected hypokalemia not amenable to correction, congenital long QT syndrome, prolonged QT interval due to medications, corrected QT based on Fridericia's formula (QTcF) \> 450 msec (for men) or \> 470 msec (for women). 3. Symptomatic heart failure (per New York Heart Association guidelines; (Caraballo, 2019), unstable angina, myocardial infarction, severe cardiovascular disease (ejection fraction \< 20%, transient ischemic attack, or cerebrovascular accident within 6 months of Day 1). 8. Participant has a history of major surgery within 4 weeks of Screening. 9. Participant has experienced bowel obstruction related to the current cancer within the last 4 weeks or signs or symptoms of intestinal obstruction, which include nausea, vomiting, or objective radiologic finding of bowel obstruction in the last 4 weeks before the start of the treatment. 10. Participant has taken a prior cell cycle CHK1 inhibitor, including ACR-368

Interventions

DRUG

ACR-368

DRUG

Gemcitabine

DIAGNOSTIC_TEST

OncoSignature

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Conditions

Endometrial Adenocarcinoma

Locations

University of South Alabama Mitchell Cancer Institute

Mobile, Alabama 36604

United States

Alaska Women's Cancer Center

Anchorage, Alaska 99508

United States

HonorHealth

Phoenix, Arizona 85016

United States

Arizona Oncology Associate, PC- HOPE

Tucson, Arizona 85711

United States

University of Arkansas for Medical Sciences

Little Rock, Arkansas 72205

United States

City of Hope National Medical Center

Duarte, California 91010

United States

UC San Diego Moores Cancer Center

La Jolla, California 92037

United States

USC/Norris Comprehensive Cancer Center

Los Angeles, California 90033

United States

Cedars Sinai Medical Center

Los Angeles, California 90048

United States

Hoag Cancer Center

Newport Beach, California 92663

United States

UC Irvine Health

Orange, California 92868

United States

Stanford Cancer Center

Palo Alto, California 94304

United States

University of California, Davis Comprehensive Cancer Center

Sacramento, California 95817

United States

University of California Los Angeles (UCLA)

Santa Monica, California 90404

United States

University of Colorado

Aurora, Colorado 80045

United States

Yale Cancer Center

New Haven, Connecticut 06520

United States

Florida Gynecologic Oncology/Regional Cancer Center

Fort Myers, Florida 33905

United States

Mount Sinai Comprehensive Cancer Center

Miami Beach, Florida 33140

United States

Emory University

Atlanta, Georgia 30322

United States

Northeast Georgia Medical Center

Gainesville, Georgia 30501

United States

Northwestern Medicine

Chicago, Illinois 60611

United States

University of Illinois Cancer Center

Chicago, Illinois 60612

United States

University of Chicago Medicine

Chicago, Illinois 60637

United States

Carle Cancer Center

Urbana, Illinois 61801

United States

Ascension St. Vicent Hospital, Inc.

Indianapolis, Indiana 46260

United States

University of Iowa

Iowa City, Iowa 52252

United States

LSU Health Sciences

New Orleans, Louisiana 70112

United States

Trials365, LLC

Shreveport, Louisiana 71103

United States

American Oncology Partners of Maryland PA

Bethesda, Maryland 20817

United States

National Institutes of Health, Clinical Center

Bethesda, Maryland 20892

United States

Holy Cross Hospital

Silver Spring, Maryland 20910

United States

Dana Farber Cancer Institute

Boston, Massachusetts 02115

United States

University of Massachusetts Chan Medical School

Worcester, Massachusetts 01605

United States

Karmanos Cancer Institute

Detroit, Michigan 48201

United States

HCA Midwest

Kansas City, Missouri 64132

United States

John Theurer Cancer Center at Hackensack University Medical Center

Hackensack, New Jersey 07601

United States

Rutgers Cancer Institute of NJ

New Brunswick, New Jersey 08903

United States

Laura & Isaac Perlmutter Cancer Center

New York, New York 10016

United States

New York Presbyterian Hospital-Columbia University Medical Center

New York, New York 10032

United States

Memorial Sloan-Kettering Cancer Center

New York, New York 10065

United States

Mount Sinai Health System

New York, New York 10128

United States

University of Rochester Medical Center

Rochester, New York 14642

United States

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina 27599

United States

FirstHealth of the Carolinas

Pinehurst, North Carolina 28374

United States

Gabrail Cancer Center

Canton, Ohio 44718

United States

Miami Valley Hospital South

Centerville, Ohio 45459

United States

University of Cincinnati Cancer Center

Cincinnati, Ohio 45267

United States

Cleveland Clinic Foundation

Cleveland, Ohio 44195

United States

Ohio State University

Hilliard, Ohio 43026

United States

Stephenson Cancer Center at OU Health

Oklahoma City, Oklahoma 73104

United States

Oncology Associates of Oregon

Eugene, Oregon 97401

United States

Oregon Health & Sciences University

Portland, Oregon 97239

United States

Fox Chase Cancer Center

Philadelphia, Pennsylvania 19111

United States

West Penn Hospital

Pittsburgh, Pennsylvania 15224

United States

Women & Infants Hospital

Providence, Rhode Island 02905

United States

Sanford Health

Sioux Falls, South Dakota 57104

United States

Texas Oncology-Dallas Presbyterian Hospital

Dallas, Texas 75231

United States

University of Texas Southwestern Medical Center

Dallas, Texas 75390

United States

Texas Oncology

Fort Worth, Texas 76104

United States

University of Texas, MD Anderson Cancer Center

Houston, Texas 77030

United States

Huntsman Cancer Institute, University of Utah

Salt Lake City, Utah 84112

United States

University of Virginia Health System

Charlottesville, Virginia 22903

United States

Virginia Commonwealth University

Richmond, Virginia 23298

United States

Swedish Cancer Center

Seattle, Washington 98104

United States

Fred Hutchinson Cancer Center

Seattle, Washington 98109

United States

Providence Sacred Heart Medical Center and Children's Hospital

Spokane, Washington 99204

United States

Summit Cancer Center

Spokane, Washington 99208

United States

Northwest Cancer Specialists, P.C.

Vancouver, Washington 98684

United States

Froedtert and Medical College of Wisconsin

Milwaukee, Wisconsin 53226

United States

Centre François Baclesse

Caen,

France

Centre Léon Bérard

Lyon,

France

Insitute de Cancérologie de l'Ouest

Saint-Herblain,

France

Institute Gustave Roussy

Villejuif,

France

KEM | Evang. Kliniken Essen-Mitte

Essen,

Germany

Universitätsklinikum Münster, Klinik für Frauenheilkunde und Geburtshilfe

Münster,

Germany

Universitätsklinikum Ulm, Frauenheilunde und Geburtshilfe

Ulm,

Germany

CRO Aviano

Aviano,

Italy

Istituto Clinico Cannizzaro Catania

Catania,

Italy

Istituto Europeo di Oncologia

Milan,

Italy

Fondazione Pascale Istituto Tumori

Naples,

Italy

Humanitas University

Pieve Emanuele,

Italy

Policlinico Gemelli

Roma,

Italy

Ospedale Mauriziano Torino

Turin,

Italy

Hospital Clínic de Barcelona

Barcelona,

Spain

Hospital Universitario Puerta de Hierro

Barcelona,

Spain

Institut Català of Oncology (ICO)

Barcelona,

Spain

Vall d'Hebron Institute of Oncology (VHIO)

Barcelona,

Spain

Hospital Universitario 12 de Octubre

Madrid,

Spain

Hospital Universitario La Paz

Madrid,

Spain

Hospital Universitario Ramón y Cajal

Madrid,

Spain

Fundacion Instituto Valenciano de Oncologia (IVO)

Valencia,

Spain