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NCT07585266PHASE3Recruiting

A Study to Investigate Velzatinib Compared With Imatinib in Adult Participants With Previously Untreated Metastatic and/or Unresectable Gastrointestinal Stromal Tumors (StrateGIST Frontline)

GlaxoSmithKline

Start Date

7/27/2026

Completion Date

9/28/2032

Summary

Gastrointestinal Stromal Tumour (GIST) is a soft tissue tumour that develops in the digestive system, most often in the stomach or small intestine. It is caused by changes in certain proteins that cause the cells to grow uncontrollably. Although current treatments may be effective, tumours may stop responding over time, highlighting the need for newer options. This study is evaluating velzatinib (GSK6042981) in participants with newly diagnosed GIST that has spread or cannot be surgically removed. Velzatinib will be compared with imatinib, the standard treatment, to assess whether it can delay disease worsening and is safe and well tolerated.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Is at least 18 years of age or the legal age of consent in the jurisdiction in which the study is taking place at the time of signing the Informed consent form (ICF). * Has histologically or cytologically confirmed GIST that is metastatic and/or surgically unresectable. * Has not received prior systemic therapy for their metastatic and/or surgically unresectable GIST. * Tumor tissue must be provided to the central laboratory. Tumor tissues may be archival (preferred) or obtained from a fresh biopsy acquired for standard of care (biopsies must be collected before randomization). * Participants must have ≥1 target lesion (TL). * All participants must use adequate contraception according to local regulations throughout the study and for a specified period after the last dose of study medication (at least 30 days for velzatinib/imatinib, or 15 days for imatinib only, as applicable, or longer if local regulations specify). * Male participants must either be abstinent or use a male condom (with a recommendation for their female partner to use highly effective contraception). They must also refrain from donating semen. * Female participants must not be pregnant or breastfeeding. 1. Those of non-childbearing potential are eligible without additional contraception. 2. Those of childbearing potential must use an acceptable, highly effective contraceptive method and have a negative pregnancy test before starting the study. The investigator will assess their pregnancy risk. * Is capable of giving signed informed consent as described in the protocol, including compliance with the requirements and restrictions listed in the ICF and in this protocol. * Has an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1. * Has adequate organ function. Exclusion Criteria: * Has a malignancy (except disease under study) that has progressed or required active treatment within the past 24 months except for basal cell or squamous cell carcinomas of the skin or in-situ carcinomas \[e.g., breast, cervix, bladder\] that have been resected with no evidence of metastatic disease. * Has any clinically significant gastrointestinal abnormalities that may alter absorption, e.g., malabsorption syndrome or major resection of the stomach and/or bowels. * Has had any major surgery (minor surgical procedures such as central venous catheter placement and tumor needle biopsy are not considered major surgical procedures) within 14 days of the first dose of study treatment or participants who have not fully recovered from surgery. * Has any history of prior allogenic or autologous bone marrow transplant or other solid organ transplant. Participants with a history of autologous stem cell transplant are eligible for study participation provided the following eligibility criteria are met: a) transplant was \[\>100 days\] prior to screening, and b) the participant has no active infection(s) at the time of screening. * Has known allergy or hypersensitivity to velzatinib or imatinib, in the opinion of the investigator or medical monitor, contraindicates participation in the study. * Has a history within 6 months prior of clinically significant or uncontrolled cardiac disease, unstable angina, acute myocardial infarction, New York Heart Association Class III or IV congestive heart failure \[New York Heart Association,1994\], or clinically significant arrhythmia not controlled by standard of care therapy, ventricular arrhythmia, cerebrovascular accident or transient ischemic attack and uncontrolled hypertension. * Has untreated brain or Central nervous system (CNS) metastases or brain/CNS metastases that have progressed \[e.g., evidence of new or enlarging brain metastasis or new neurologic symptoms attributable to brain/CNS metastases\]. Participants with previously treated and clinically stable brain/CNS metastases and who have completed all corticosteroid therapy for ≥2 weeks before randomization are not excluded from participation * Has ongoing adverse reaction(s) from prior therapy that has (have) not recovered to ≤Grade 1 or to the baseline status preceding prior therapy, (excluding e.g., alopecia, hearing loss, vitiligo, endocrinopathy managed with replacement therapy, and Grade 2 neuropathy) or that the investigator, with the agreement of the sponsor, considers to be not clinically relevant for the tolerability of study intervention in the current clinical study. * Has any active renal condition (e.g., infection, requirement for dialysis, or any other significant renal condition that could affect the participant's safety). * Has any serious and/or unstable medical or psychiatric disorder or other condition(s) (including laboratory assessment abnormalities) that could interfere with the participant's safety, obtainment of informed consent, or compliance to the study procedures. * Has received radiotherapy within 14 days prior to first dose of study treatment. * Has received any live vaccine within 30 days of randomization. Vaccination against Coronavirus disease 2019 (COVID-19) using vaccines that are authorized via the appropriate regulatory mechanisms (e.g., Emergency Use Authorization, Conditional Marketing Authorization, or Marketing Authorization Application) are not exclusionary. * Has received any transfusion of blood products (including platelets or red blood cells) or administration of colony-stimulating factors (including Granulocyte colony-stimulating factor \[G-CSF\], granulocyte macrophage colony-stimulating factor, or recombinant erythropoietin) within 14 days before randomization. * Is currently enrolled or has participated in any other clinical study involving an investigational study intervention or any other type of medical research before signing ICF. * Has a positive drug/alcohol screening assessment. * Has a known Human immunodeficiency virus (HIV) infection and meets at least one of the following criteria: 1. Has documented evidence of plasma HIV-1 ribonucleic acid (RNA) ≥50 c/mL within 3 months prior to or at screening. In the 3 to 12 months prior to screening, plasma HIV 1 RNA levels consistently \<50 c/mL are required for enrollment; if multiple instances of plasma HIV-1 RNA values ≥50 c/mL occurred in the 3 to 12 months prior to screening, the participant is not eligible for enrollment unless, per the investigator's assessment, the elevations were neither persistent nor associated with antiretroviral resistance; OR 2. Has not had CD4 cell counts measured in the past 12 months (i.e., at least two separate measurements taken a minimum of 28 days apart, one of which must be conducted at screening); OR 3. Has had any CD4 cell count values ≤200 cells/mm3 in the past 12 months; OR 4. Has had one or more changes in their combination antiretroviral therapy regimen (except for switches as allowed per details provided in protocol) or has received an antiretroviral therapy regimen that is inconsistent with locally recommended guidelines during the 3 months prior to screening; OR 5. Has a history of HIV-associated non-Hodgkin lymphoma within 5 years prior to screening or a history of HIV-associated invasive cervical cancer; OR 6. Has received treatment with an HIV 1 immunotherapeutic vaccine within 90 days of screening. * Is pregnant or breastfeeding. * Is unable to adhere to the protocol, including requirements for the Follow-up Period of the study. * Has an alanine aminotransferase (ALT) value \>2.5x upper limit of normal (ULN) or (for participants with documented liver metastases/tumor infiltration) has an ALT value \>5x ULN * Has a total bilirubin value \>1.5x ULN. * Has cirrhosis or current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal/gastric varices, or persistent jaundice. * Evidence of chronic hepatitis B virus (HBV) infection with detectable viral load despite antiviral therapy with high resistance barrier. * 12-lead electrocardiogram (ECG) demonstrating mean QT interval corrected (QTc) corrected by Fridericia's formula \>480msec at screening or history of long QT syndrome.

Interventions

DRUG

Velzatinib

DRUG

Imatinib

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Conditions

Gastrointestinal Stromal Neoplasms

Locations

GSK Investigational Site

Scottsdale, Arizona 85258

United States

GSK Investigational Site

San Francisco, California 94158

United States

GSK Investigational Site

New Haven, Connecticut 06510-3206

United States

GSK Investigational Site

Bethesda, Maryland 20817-1802

United States

GSK Investigational Site

Omaha, Nebraska 68130-2042

United States

GSK Investigational Site

New York, New York 10065

United States

GSK Investigational Site

Canton, Ohio 44718

United States

GSK Investigational Site

Knoxville, Tennessee 37920

United States

GSK Investigational Site

Seattle, Washington 98109-4405

United States

GSK Investigational Site

Buenos Aires, 1425

Argentina

GSK Investigational Site

Capital Federal, C1426ANZ

Argentina

GSK Investigational Site

Ciudad Autonoma de Buenos Aire, C1414DRK

Argentina

GSK Investigational Site

Ciudad Autonoma de Buenos Aire, C1431FWO

Argentina

GSK Investigational Site

Ciudad autOnoma de Bueno, C1419AHN

Argentina

GSK Investigational Site

San Miguel de Tucumán, T4000IHE

Argentina

GSK Investigational Site

Melbourne, Victoria 3004

Australia

GSK Investigational Site

Teresina, Piauí 64002-530

Brazil

GSK Investigational Site

Barretos, 14784-400

Brazil

GSK Investigational Site

Florianópolis, 88034-000

Brazil

GSK Investigational Site

Natal, 59075-740

Brazil

GSK Investigational Site

Porto Alegre, 90020-090

Brazil

GSK Investigational Site

Vitória, 29043-260

Brazil

GSK Investigational Site

Toronto, Ontario M5G 2M9

Canada

GSK Investigational Site

Montreal, Quebec H3A 1A1

Canada

GSK Investigational Site

Beijing, 100141

China

GSK Investigational Site

Chengdu, 610041

China

GSK Investigational Site

Guangzhou, 510060

China

GSK Investigational Site

Guangzhou, 510080

China

GSK Investigational Site

Guangzhou, 510655

China

GSK Investigational Site

Hangzhou, 310016

China

GSK Investigational Site

Jinan, 250021

China

GSK Investigational Site

Shanghai, 20001

China

GSK Investigational Site

Wuhan, 430022

China

GSK Investigational Site

Zhengzhou, 450052

China

GSK Investigational Site

Reims, 51100

France

GSK Investigational Site

Chaïdári, Attica 124 62

Greece

GSK Investigational Site

Thessaloniki, 55535

Greece

GSK Investigational Site

Milan, 20141

Italy

GSK Investigational Site

Ehime, 791-0280

Japan

GSK Investigational Site

Fukuoka, 812-8582

Japan

GSK Investigational Site

Gifu, 501-1194

Japan

GSK Investigational Site

Hokkaido, 060-8648

Japan

GSK Investigational Site

Kanagawa, 241-8515

Japan

GSK Investigational Site

Osaka, 565-0871

Japan

GSK Investigational Site

Tokyo, 104-0045

Japan

GSK Investigational Site

Toyama, 930-0194

Japan

GSK Investigational Site

Yamaguchi, 755-8505

Japan

GSK Investigational Site

Nijmegen, 6525GA

Netherlands

GSK Investigational Site

Oslo, 0379

Norway

GSK Investigational Site

Seoul, Seoul Teugbyeolsi 06351

South Korea

GSK Investigational Site

Seongnam-si Gyeonggi-do, 13620

South Korea

GSK Investigational Site

Seoul, 03080

South Korea

GSK Investigational Site

Seoul, 03181

South Korea

GSK Investigational Site

Seoul, 03722

South Korea

GSK Investigational Site

Seoul, 138-736

South Korea

GSK Investigational Site

Suwon Kyunggi-do, 16499

South Korea

GSK Investigational Site

BaracaldoVizcaya, 48903

Spain

GSK Investigational Site

Barcelona, 8025

Spain

GSK Investigational Site

Madrid, 28034

Spain

GSK Investigational Site

Madrid, 28040

Spain

GSK Investigational Site

Madrid, 28041

Spain

GSK Investigational Site

Madrid, 28046

Spain

GSK Investigational Site

Seville, 41013

Spain

GSK Investigational Site

Zaragoza, 50009

Spain

GSK Investigational Site

Changhua, 500

Taiwan

GSK Investigational Site

Taichung, 404

Taiwan

GSK Investigational Site

Taipei, 10002

Taiwan

GSK Investigational Site

Taipei, 112

Taiwan

GSK Investigational Site

Taoyuan, 33305

Taiwan

GSK Investigational Site

London, NW1 2PG

United Kingdom

GSK Investigational Site

London, SW3 6JJ

United Kingdom

GSK Investigational Site

Sheffield, S10 2SJ

United Kingdom