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Spots Global Cancer Trial Database for 9-ING-41 in Patients With Advanced Cancers

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Trial Identification

Brief Title: 9-ING-41 in Patients With Advanced Cancers

Official Title: Phase 1/2 Study of 9-ING-41, a Glycogen Synthase Kinase-3 Beta (GSK-3β) Inhibitor, as a Single Agent and Combined With Chemotherapy, in Patients With Refractory Hematologic Malignancies or Solid Tumors

Study ID: NCT03678883

Study Description

Brief Summary: GSK-3β is a potentially important therapeutic target in human malignancies. The Actuate 1801 Phase 1/2 study is designed to evaluate the safety and efficacy of 9-ING-41, a potent GSK-3β inhibitor, as a single agent and in combination with cytotoxic agents, in patients with refractory cancers.

Detailed Description: 9-ING-41 is a first-in-class, intravenously administered, maleimide-based small molecule potent selective GSK-3β inhibitor with significant pre-clinical antitumor activity. GSK-3 is a serine/threonine kinase initially described as a key regulator of metabolism and has a role in diverse disease processes including cancer, immune disorders, pathologic fibrosis, metabolic disorders, and neurological disorders. GSK-3 has two ubiquitously expressed and highly conserved isoforms, GSK-3α and GSK-3β, with both shared and distinct substrates and functional effects. GSK-3β is particularly important in tumor progression and modulation of oncogenes (including beta-catenin, cyclin D1 and c-Myc), cell cycle regulators (e.g. p27Kip1) and mediators of epithelial-mesenchymal transition (e.g. zinc finger protein SNAI1, Snail). Aberrant overexpression of GSK-3β has been shown to promote tumor growth and chemotherapy resistance in various solid tumors including colon, ovarian, and pancreatic cancers and glioblastoma through differential effects on the pro-survival nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and c-Myc pathways as well on tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and p53-mediated apoptotic mechanisms. GSK-3β helps maintain malignant cell survival and proliferation, particularly in terms of mediating resistance to standard anti-cancer therapies, through the NF-κB pathway. GSK-3β has been established as a potential anticancer target in human bladder, breast, colorectal, glioblastoma, lung, neuroblastoma, ovarian, pancreatic, prostate, renal and thyroid cancers as well as chronic lymphocytic leukemia and lymphomas. 9-ING-41 is a small molecule potent selective GSK-3β inhibitor with broad spectrum pre-clinical antitumor activity. It's modes of action include downregulation of NF-κB and decreasing the expression NF-κB target genes including cyclin D1, Bcl-2, anti-apoptotic protein (XIAP) and B-cell lymphoma-extra large (Bcl-XL) leading to inhibition of tumor growth in multiple solid tumor cell and lymphoma lines and patient derived xenograft (PDX) models. NF-κB is constitutively active in cancer cells and promotes anti-apoptotic molecule expression. NF-κB activation is particularly important in cancer cells that have become chemo- and/or radio-resistant. 9-ING-41 also has significant activity in pre-clinical models of pathological pleural and pulmonary fibrosis. 9-ING-41 has significant in vitro and in vivo activity as a single agent and/or in combination with standard cytotoxic chemotherapies in a spectrum of solid tumors and hematological malignancies including bladder, breast, glioblastoma, neuroblastoma, pancreatic, sarcomas, and renal cancers as well as lymphomas. The 1801 had three parts: * Completed: Part 1 (9-ING-41 as monotherapy): The standard 3+3 dose escalation design will be applied to all dose cohorts until the Maximum Tolerated Dose (MTD) or Recommended Phase 2 Dose (RP2D) is identified. * Completed: 9-ING-41 combined with standard anticancer agents: The 3+3 dose escalation study design will be used for 8 chemotherapy combination regimens (9-ING-41 plus gemcitabine, doxorubicin, lomustine, carboplatin, irinotecan, nab-paclitaxel plus gemcitabine, paclitaxel plus carboplatin, pemetrexed plus carboplatin) to identify the MTD/RP2D of each regimen. * Part 3: A randomized Phase 2 study of 9-ING-41 either once or twice weekly with gemcitabine and nab-paclitaxel (GA) versus GA alone for patients with previously untreated metastatic or locally advanced pancreatic cancer is now open.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic, Phoenix, Arizona, United States

Arizona Oncology Associates, Tucson, Arizona, United States

The University of Arizona Cancer Center, Tucson, Arizona, United States

University of California Irvine Health, Orange, California, United States

UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States

Christiana Care Health Services, Newark, Delaware, United States

Sibley Memorial Hospital, Washington, District of Columbia, United States

Florida Cancer Specialists - South, Fort Myers, Florida, United States

Miami Cancer Institute, Miami, Florida, United States

Florida Cancer Specialists - North, Saint Petersburg, Florida, United States

Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, United States

Des Moines Oncology Research Association, Des Moines, Iowa, United States

Kansas University Cancer Center, Kansas City, Kansas, United States

Ochsner Clinic Foundation, New Orleans, Louisiana, United States

University of Michigan, Ann Arbor, Michigan, United States

MetroMetro-Minnesota Community Oncology Research Consortium (MMCORC), Minneapolis, Minnesota, United States

Mayo Clinic, Rochester, Minnesota, United States

Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States

Morristown Medical Center, Morristown, New Jersey, United States

Capital Health Medical Center/ Hopewell, Pennington, New Jersey, United States

MD Anderson Cancer Center at Cooper, Voorhees, New Jersey, United States

Columbia University- Irving Medical Center, New York, New York, United States

Stony Brook University Hospital, Stony Brook, New York, United States

Duke University Medical Center, Durham, North Carolina, United States

Oregon Health and Science University, Portland, Oregon, United States

St. Luke's University Health Network, Bethlehem, Pennsylvania, United States

Allegheny Health Network, Pittsburgh, Pennsylvania, United States

Rhode Island Hospital, Providence, Rhode Island, United States

Prisma Health Cancer Institute, Greenville, South Carolina, United States

Sanford Research, Sioux Falls, South Dakota, United States

West Cancer Center, Germantown, Tennessee, United States

Baptist Clinical Research Institute, Memphis, Tennessee, United States

Sarah Cannon Research Institute- Tennessee Oncology-Nashville, Nashville, Tennessee, United States

Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States

Texas Oncology- Charles A. Sammons Cancer Center, Dallas, Texas, United States

UT Southwestern Medical Center, Dallas, Texas, United States

Utah Cancer Specialists, Salt Lake City, Utah, United States

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States

West Virginia University, Morgantown, West Virginia, United States

UW Carbone Cancer Center, Madison, Wisconsin, United States

UZA- Antwerpen, Edegem, Antwerp, Belgium

Imelda VZW, Bonheiden, , Belgium

UZ Gent, Gent, , Belgium

UZ Leuven Gasthuisberg, Leuven, , Belgium

Cross Cancer Institute, Edmonton, Alberta, Canada

QE II Health Sciences Centre, Halifax, Nova Scotia, Canada

Centre Intégré de Santé et de Services Sociaux de la Montérégie-Centre, Greenfield Park, Quebec, Canada

Jewish General Hospital, Montréal, Quebec, Canada

McGill University Health Centre, Montréal, Quebec, Canada

Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada

Center Hospitalier Regional Universitaire de Besancon - Site Jean Minjoz, Besançon, Bourgogne-Franche-Comte, France

CHRU Brest Hopital Morvan, Brest, Bretagne, France

Hopital Claude Huriez, Lille, Hauts De France, France

Institute de Cancerologie de Lorraine, Vandœuvre-lès-Nancy, Meurthe-et-Moselle, France

Institut Bergonie, Bordeaux, Nouvelle Aquitaine, France

Insitut de Cancerologie de l'Ouest, Saint-Herblain, Pays-de-la-Loire, France

Hopital de la Timone, Marseille, , France

Netherlands Cancer Institute, Amsterdam, , Netherlands

Fundacao Champalimaud, Lisbon, , Portugal

Hospital Da Luz, Lisbon, , Portugal

Centro Hospitalar Universitario Sao Joao, Porto, , Portugal

Vall d'Hebron Institute of Oncology, Barcelona, , Spain

Institut Catala d'Oncologia, Barcelona, , Spain

Hospital Clinico U San Carlos (HSC), Madrid, , Spain

START Madrid-HM CIOCC Hospital Universitario, Madrid, , Spain

INCLIVA University of Valencia, Valencia, , Spain

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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