New hope for stomach cancer: targeted drug combo enters final testing

NCT ID NCT07385703

Disease control Sponsor: Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd. Source: ClinicalTrials.gov ↗

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This Phase 3 trial is testing whether a new drug combination (tecotabart vedotin plus tislelizumab) works better than standard chemotherapy for people with advanced stomach cancer that has a specific protein called CLDN18.2. The study plans to enroll 752 participants who have not had prior treatment for their advanced cancer. The main goal is to see if the new combo delays cancer growth and improves survival.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance: tecotabart vedotin (LM-302) plus tislelizumab
What this could lead to: If successful, this could offer a new first-line treatment option for people with advanced stomach cancer that targets a specific protein (CLDN18.2), potentially improving how long they live without their cancer growing.
What could go wrong: This is an early-stage Phase 3 trial, so results are not yet known. The new drug combination may not work better than current chemotherapy, and side effects from the targeted therapy and immunotherapy could be significant.

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 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

About 752 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2026

Expected to finish

May 2030

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 years and older

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Willing and able to comply with the study's visit schedule, treatment plan, laboratory tests, and other research procedures. * Age ≥ 18 years. * Histologically or cytologically confirmed adenocarcinoma of the stomach or gastroesophageal junction. * For locally advanced unresectable or metastatic adenocarcinoma of the stomach or gastroesophageal junction that has not previously received any systemic treatment: * Patients who have previously received radical neoadjuvant chemotherapy or adjuvant chemotherapy (radiotherapy) based on a platinum-based combination chemotherapy regimen and have not developed distant metastasis or local recurrence within 6 months after completion of treatment can be included. * The calculation of a 6-month interval is defined as recurrence within the same date range after 6 months. For example, if the end date of the last treatment is January 1, the 6-month period from that date refers to January 1 to July 1 (including July 1). Alternatively, if the end date of the last treatment is August 31, the 6-month period from that date refers to August 31 to February 28 (or February 29 in leap years). * Archived specimens or fresh tumor tissue specimens from ≤3 years ago must be provided for CLDN18.2 and PD-L1 testing (PD-L1 results are not a condition for enrollment). When multiple samples are present, the most recent accessible and qualified sample must be provided. After confirmation by the central laboratory, tumor tissue with positive CLDN18.2 expression is defined as ≥25% tumor cell membrane staining intensity 2+ \& 3+. For patients who have previously received radical neoadjuvant chemotherapy or adjuvant chemotherapy (radiotherapy) based on platinum-containing combination chemotherapy regimens, newly obtained tissue from recurrent or metastatic lesions must be provided for CLDN18.2 and PD-L1 testing. * A negative report on the expression detection of human epidermal growth factor receptor-2 (HER2) in tumor tissue must be provided. The definition of HER2 negative expression is ImmunoHistoChemistry (IHC) score 0/1+, IHC score 2+, and fluorescence in situ hybridization (FISH) negative. * According to the RECIST 1.1 evaluation criteria, there must be at least one measurable lesion. * Expected survival duration ≥ 3 months. * According to the Eastern Cooperative Oncology Group (ECOG) standards, the physical performance status score is 0 or 1. * Good organ function: a. Bone marrow reserve: Platelets (PLT) ≥ 100×10\^9/L, absolute neutrophil count (ANC) ≥ 1.5×10\^9/L, Hemoglobin (Hb) ≥ 90 g/L (no blood transfusion or supportive treatment such as colony-stimulating factors within 14 days prior to hematology parameter examination during the screening period); b. Coagulation function: International normalized ratio (INR) ≤ 1.5, Activated partial thromboplastin time (APTT) ≤ 1.5×upper limit of normal (ULN); c. Liver function: Total bilirubin ≤ 1.5×ULN, Alanine aminotransferase (ALT), Aspartate aminotransferase (AST), Alkaline phosphatase (ALP) ≤ 2.5×ULN (if there is liver metastasis, then ALT and AST ≤ 5×ULN) and Albumin (ALB) ≥ 30 g/L; d. Renal function: Creatinine clearance rate ≥ 50 mL/min (calculated according to the Cockcroft-Gault formula); e. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%; QT interval (QTcF) ≤ 470 ms for females and ≤ 450 ms for males. * Women of childbearing age must have a negative blood pregnancy test within 7 days before administration; any fertile male and female subjects must agree to use highly effective contraception throughout the study medication period and for 7 months after the last dose of the study. Males must agree to refrain from donating sperm during the study period and for 7 months after the last dose of the study. Females must agree to refrain from breastfeeding during the study period. Exclusion Criteria: * Other pathological types confirmed by histopathology, such as squamous cell carcinoma, sarcoma, or undifferentiated carcinoma. * There are gastric cancer lesions confirmed by imaging that are accompanied by cavities or necrosis, and are closely related to major blood vessels, and are assessed by the researchers as posing a high risk of major bleeding. * Patients with known central nervous system (CNS) metastases. Patients with non-meningeal, midbrain, pontine, or spinal cord metastases who are judged by the investigator to have stable brain metastases can be enrolled. Stable brain metastases are defined as patients whose brain metastases have undergone treatment and the condition of the metastases has stabilized (brain imaging examination at least 28 days before randomization shows stable lesions, no neurological symptoms, and no immediate need for local or systemic treatment within 14 days before randomization), with no evidence of new or previously existing brain metastases enlarging. * Clinically uncontrollable third-space effusion, such as moderate or greater volume, requiring long-term catheterization, previous history of intestinal obstruction or paralysis, compartmented ascites, undergoing or planning to undergo local treatment (including drainage, peritoneal shunt, or cell-free concentrated ascites reinfusion therapy) within 14 days prior to screening, or significant increase within 2 weeks after local treatment, meeting any of the above criteria or deemed unsuitable for enrollment by the investigator. * Patients with symptomatic spinal cord compression, or those who are expected to develop symptoms of spinal cord compression if left untreated; or for patients with previously diagnosed and treated spinal cord compression, there is no evidence indicating that the disease was clinically stable for ≥4 weeks before the first study drug administration; except for patients with asymptomatic spinal cord compression indicated by imaging, who are assessed as stable by a specialist and do not require treatment for spinal cord compression at this time. * Accompanied by severe peritoneal metastasis, the main manifestations are: clinically significant intestinal obstruction; barium enema indicating small intestinal stenosis. * History of gastrointestinal perforation or gastrointestinal fistula within the previous 6 months. If the perforation or fistula has been treated through resection or repair surgery, and the condition is assessed by the investigator as having been cured or controlled, participation in the study is permissible. * Poorly controlled tumor-related pain: * For patients requiring analgesic treatment, a stable dosage of treatment must be established before participating in the study. * Symptomatic lesions suitable for palliative radiotherapy (such as bone metastasis or metastasis causing nerve damage) should be treated before enrollment. * Before enrollment, if appropriate, consideration should be given to local treatment for asymptomatic metastatic lesions that may lead to functional deficits or intractable pain due to further growth (e.g., epidural metastasis not currently associated with spinal cord compression). * Patients with a body weight of less than 35kg or a body weight loss of more than 10% within 2 months prior to signing the informed consent form. Exclusion criteria for comorbidities or concomitant conditions: * History of malignancy other than Gastric Cancer (GC)/GastroEsophageal Junction adenocarcinoma (GEJ) adenocarcinoma within 2 years prior to randomization, with the following exceptions: basal cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, squamous cell carcinoma of the skin, etc., which have been completely cured and treated. * History of autoimmune diseases, including but not limited to: myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis. The following conditions are excluded: • Subjects with autoimmune-related hypothyroidism who are receiving stable-dose thyroid hormone replacement therapy. * Subjects with type 1 diabetes who are well-controlled under a stable insulin treatment regimen. * Only subjects with skin autoimmune diseases that do not require systemic treatment (such as vitiligo, alopecia, psoriasis, or eczema). * Subjects who have recovered from childhood asthma and do not require any intervention in adulthood. * Subjects whose relevant diseases, as assessed by the researchers, are unlikely to recur without external triggers. * Patients who have previously undergone allogeneic bone marrow transplantation or solid organ transplantation. * Patients with a history of severe cardiovascular and cerebrovascular diseases, including but not limited to: * Severe cardiac rhythm or conduction abnormalities, such as arrhythmias requiring clinical intervention, second- or third-degree atrioventricular block, left bundle branch block, prolonged QRS complex, etc.; * Patients with thromboembolic events requiring therapeutic anticoagulation, or those with venous filters; * Patients with heart failure of New York Heart Association (NYHA) class III or IV; * Patients who have experienced acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other cardiovascular and cerebrovascular events of grade 3 or above within the previous 6 months prior to randomization. * Have a history of myocarditis or cardiomyopathy. * For individuals infected with human immunodeficiency virus (HIV) and those with active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection, the following conditions are allowed for enrollment: • Patients who are HBsAg positive, with or without HBcAb positivity, and have HBV DNA \< 500 IU/mL or below the lower limit of the reference value set by the research center, and who, based on clinical treatment, manifestations, and other factors, are judged by the investigator to have no active infection; • Patients who are HCV antibody positive but HCV RNA negative. * Subjects with known active syphilis infection. * Individuals who are unable to control themselves or have severe illnesses, including but not limited to active infections requiring systemic antibiotic treatment within 2 weeks before the first dose, and interstitial pneumonia/lung disease requiring intervention during screening. * Subjects with known active tuberculosis. For patients suspected of having active tuberculosis, a comprehensive evaluation should be conducted based on chest imaging, sputum smear/culture, or molecular testing results, as well as clinical symptoms and signs, to make a definitive diagnosis. * Currently present peripheral sensory or motor neuropathy of ≥ grade 2. * Subjects who received systemic corticosteroids (\>10mg/d prednisone equivalent) or other systemic immunosuppressants (including but not limited to cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor drugs \[anti-Tumor Necrosis Factor (TNF)\] within 2 weeks prior to the first study drug administration. * Topical, ocular, intra-articular, intranasal, and inhaled corticosteroids are allowed; * Patients receiving acute low-dose systemic immunosuppressive drugs (e.g., single-dose dexamethasone for nausea); * Patients requiring baseline and subsequent MRI/CT tumor assessments who have previously experienced allergic reactions to intravenous contrast agents may receive prophylactic steroids; * Inhaled corticosteroids are allowed for the treatment of chronic obstructive pulmonary disease, hydrocortisone for the treatment of orthostatic hypotension, and low-dose corticosteroid hormone maintenance therapy for adrenal insufficiency. * There are factors that affect the application and absorption of oral medications, such as dysphagia, clinically uncontrollable persistent and recurrent vomiting (such as caused by gastric outlet obstruction), intestinal obstruction, and chronic diarrhea. 21. Within 28 days before randomization, there was uncontrollable/severe gastrointestinal bleeding, active peptic ulcer, or active gastrointestinal inflammation/infectious diseases (such as active diverticulitis, abdominal abscess). Subjects who have not undergone radical surgical resection of the primary lesion must undergo fecal occult blood testing before enrollment. If the result is positive, further evaluation, including but not limited to gastroscopy, is required before medication administration to confirm the presence of active bleeding from the lesion and assess the risk of bleeding. * The adverse reactions from previous anti-tumor treatment within the 14 days prior to randomization have not yet recovered to a level of ≤ grade 1 according to the Common Terminology Criteria for Adverse Events (CTCAE) v6.0 grading system (excluding toxicities that the investigator deems to pose no safety risk, are asymptomatic, or are controllable with stable medication, such as hair loss, long-term toxicity caused by radiotherapy, and other toxicities that are ≤ grade 2). * Have a history of allergy to LM-302, Ticagrelor, any control drug, or its excipients. * Individuals with known mental illnesses or disorders that may affect trial compliance. Exclusion criteria related to drug treatment: * Within 28 days prior to randomization, the subject is currently participating or has previously participated in any investigational drug study, or has used an investigational device within 28 days. Subjects who have entered the follow-up period of an investigational drug study and have not used the investigational drug for ≥28 days since the last use may meet the inclusion criteria for this study. * Previously received targeted therapy targeting CLDN18.2, such as antibody-drug conjugate (ADC) therapy, antibody therapy, and chimeric antigen receptor T-cell (CAR-T) therapy; previously received ADC therapy using small molecule toxin Monomethyl auristatin E (MMAE). * Subjects who have received palliative local treatment (such as radiotherapy or surgery) for non-target lesions within 2 weeks prior to the first dose, or who have previously received radiotherapy for locally advanced unresectable or metastatic gastric cancer or GEJ adenocarcinoma and have not recovered from toxicity within 2 weeks prior to randomization. * Within the first 2 weeks before randomization, patients received systemic treatment with traditional Chinese patent medicines and simple preparations with anti-tumor indications, or with Chinese herbal medicine, or with drugs with immune regulatory effects (including thymosin, interferon, interleukin, etc.). * Having undergone or planning to undergo major surgery or interventional therapy (excluding tumor biopsy, puncture, etc.) within the 28 days prior to randomization or during the study period. * Use of strong inhibitors/strong inducers of CYP3A4 within 14 days before randomization; * Vaccination with any live vaccine or attenuated live vaccine within 28 days before randomization. * Other situations where the researcher deems it inappropriate for participation in this study.

Get updates

Get notified about this study

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

adenocarcinoma gastric adenocarcinoma gastroesophageal junction adenocarcinoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Adenocarcinoma

How to take part

Only the study team decides who joins. These are the ways to reach them.

The places running it

106 sites. The list below names each one and where it is.
The official record

ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

Open the record ↗
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

Affiliated Cancer Hospital of Harbin Medical University
NOT_YET_RECRUITING

Harbin, Heilongjiang, 150081, China
Affiliated Hospital Of Ji Ning Medical University
NOT_YET_RECRUITING

Jining, Shandong, 272029, China
Affiliated Hospital of Chengde Medical University
NOT_YET_RECRUITING

Chengde, Hebei, 067000, China
Affiliated Hospital of North Sichuan Medical College
NOT_YET_RECRUITING

Nanchong, Sichuan, 637000, China
Affiliated Hospital of Yangzhou Univrtsity
NOT_YET_RECRUITING

Yangzhou, Jiangsu, 225000, China
Affiliated Tumor Hospital of Xinjiang Medical University
NOT_YET_RECRUITING

Ürümqi, Xinjiang, 830000, China
Affiliated Zhongshan Hospital Of Dalian University
NOT_YET_RECRUITING

Dalian, Liaoning, 116001, China
Anhui Provincial Cancer Hospital
NOT_YET_RECRUITING

Hefei, Anhui, 230000, China
Anhui Provincial Cancer Hospital
NOT_YET_RECRUITING

Hefei, Anhui, 230000, China
Anhui Provincial Hospital (The First Affiliated Hospital of China University of Science and Technology)
NOT_YET_RECRUITING

Hefei, Anhui, 230000, China
Anyang Cancer Hospital
NOT_YET_RECRUITING

Anyang, Henan, 455000, China
Baoji Central Hospital
NOT_YET_RECRUITING

Baoji, Shaanxi, 721008, China
Beijing Cancer Hospital
RECRUITING

Beijing, Beijing Municipality, 100142, China
Beijing Friendship Hospital, Capital Medical University
NOT_YET_RECRUITING

Beijing, Beijing Municipality, 100050, China
Beijing Gaobo Hospital Co., Ltd.
NOT_YET_RECRUITING

Beijing, Beijing Municipality, 102200, China
Beijing Lu He Hospital ,Capital Medical University
NOT_YET_RECRUITING

Beijing, Beijing Municipality, 101149, China
Beijing Tsinghua changgung Hospital
NOT_YET_RECRUITING

Beijing, Beijing Municipality, 102218, China
Cancer Hospital of Shandong First Medical University (Shandong Cancer Institute, Shandong Cancer Hospital)
NOT_YET_RECRUITING

Jinan, Shandong, 250000, China
Chang zhi People's Hospital
NOT_YET_RECRUITING

Changzhi, Shanxi, 046000, China
Chifeng Municipal Hospital
NOT_YET_RECRUITING

Chifeng, Inner Mongolia, 24000, China
China-Japan Union Hospital of Jilin University
NOT_YET_RECRUITING

Changchun, Jilin, 130000, China
Chongqing University Three Gorges Hospital
NOT_YET_RECRUITING

Chongqing, Chongqing Municipality, 404000, China
First Hospital Of Shan Xi Medical University
NOT_YET_RECRUITING

Taiyuan, Shanxi, 30001, China
Fudan University Shanghai Cancer Center
NOT_YET_RECRUITING

Shanghai, Shanghai Municipality, 201321, China
Fujian Cancer Hospital
NOT_YET_RECRUITING

Fuzhou, Fujian, 350000, China
Fujian Medical University Union Hospital
NOT_YET_RECRUITING

Fuzhou, Fujian, 350000, China
Fujian Provincial Hospital
NOT_YET_RECRUITING

Fuzhou, Fujian, 350000, China
Gansu Provincial Cancer Hospital
NOT_YET_RECRUITING

Lanzhou, Gansu, 730050, China
Gansu Provincial Hospital
NOT_YET_RECRUITING

Lanzhou, Gansu, 730000, China
Gansu Wuwei Tumour Hospital
NOT_YET_RECRUITING

Wuwei, Gansu, 730000, China
Guangdong provincial people's hospital
NOT_YET_RECRUITING

Guangzhou, Guangdong, 510080, China
Guangxi Medical University Afiliated Tomor Hospital
NOT_YET_RECRUITING

Nanning, Guangxi, 530000, China
Guigang City People's Hospital
NOT_YET_RECRUITING

Guigang, Guangxi, 537100, China
Hainan general hospital
NOT_YET_RECRUITING

Haikou, Hainan, 570311, China
Henan Provincial Cancer Hospital
NOT_YET_RECRUITING

Zhengzhou, Henan, 450003, China
Hubei Cancer Hospital
NOT_YET_RECRUITING

Wuhan, Hubei, 430079, China
Hunan Cancer Hospital
NOT_YET_RECRUITING

Changsha, Hunan, 410000, China
Hunan Cancer Hospital
NOT_YET_RECRUITING

Changsha, Hunan, 410000, China
Jiamusi Tuberculosis Hospital (Jiamusi Cancer Hospital)
NOT_YET_RECRUITING

Jiamusi, Heilongjiang, 154002, China
Jiangsu Province Hospital
NOT_YET_RECRUITING

Nanjing, Jiangsu, 210029, China
Jiangsu Provincial Cancer Hospital
NOT_YET_RECRUITING

Nanjing, Jiangsu, 210009, China
Jiangxi Cancer Hospital
NOT_YET_RECRUITING

Nanchang, Jiangxi, 330029, China
Jilin Cancer Hospital
NOT_YET_RECRUITING

Changchun, Jilin, 130000, China
Jinan Central Hospital (City level)
NOT_YET_RECRUITING

Jinan, Shandong, 250000, China
Jingzhou First People's Hospital
NOT_YET_RECRUITING

Jingzhou, Hubei, 430000, China
Liaoning Cancer Hospital & Institute
NOT_YET_RECRUITING

Shenyang, Liaoning, 110801, China
Linyi Cancer Hospital
NOT_YET_RECRUITING

Linyi, Shandong, 276034, China
Linyi People's Hospital
NOT_YET_RECRUITING

Linyi, Shandong, 276000, China
Lishui Central Hospitall
NOT_YET_RECRUITING

Lishui, Zhejiang, 323000, China
Luoyang Central Hospital
NOT_YET_RECRUITING

Luoyang, Henan, 471000, China
Meizhou People's Hospital
NOT_YET_RECRUITING

Meizhou, Guangdong, 514000, China
Nanchang University First Affiliated Hospital
NOT_YET_RECRUITING

Nanchang, Jiangxi, 330006, China
Nanjing Drum Tower Hospital
NOT_YET_RECRUITING

Nanjing, Jiangsu, 210009, China
Nantong Tumor Hospital
NOT_YET_RECRUITING

Nantong, Jiangsu, 226300, China
Nanyang Second General Hospital
NOT_YET_RECRUITING

Nanyang, Henan, 473000, China
Peking University Cancer Hospital Inner Mongolia Hospita
NOT_YET_RECRUITING

Hohhot, Inner Mongolia, 010000, China
Qingdao Municipal Hospital (Group)
NOT_YET_RECRUITING

Qingdao, Shandong, 266100, China
QinghaiI University Affiliated Hospital
NOT_YET_RECRUITING

Xining, Qinghai, 810000, China
Shaanxi Provincial People's Hospital
NOT_YET_RECRUITING

Xi'an, Shaanxi, 710000, China
Shanghai General Hospital
NOT_YET_RECRUITING

Shanghai, Shanghai Municipality, 200001, China
Shanghai GoBroad Cancer Hospital China Pharmaceutical University
NOT_YET_RECRUITING

Shanghai, Shanghai Municipality, 200131, China
Shantou University Medical College Affiliated Tumor Hospital
NOT_YET_RECRUITING

Shantou, Guangdong, 515000, China
Shanxi Cancer Hospital
NOT_YET_RECRUITING

Taiyuan, Shanxi, 030000, China
Shengjing Hospital of China Medical University
NOT_YET_RECRUITING

Shenyang, Liaoning, 110001, China
Sichuan Academy of Medical Science&Sichuan Provincial People' Hospital
NOT_YET_RECRUITING

Chengdu, Sichuan, 610000, China
Sichuan Provincial Cancer Hospital
NOT_YET_RECRUITING

Chengdu, Sichuan, 610041, China
Sir Run Run Shaw Hospital Zhejiang University School of Medicine
NOT_YET_RECRUITING

Hangzhou, Zhejiang, 310016, China
Subei People's Hospital of Jiangsu province
NOT_YET_RECRUITING

Yangzhou, Jiangsu, 225001, China
The Affiliated Hospital of Inner Mongolia Medical University
NOT_YET_RECRUITING

Hohhot, Inner Mongolia, 010000, China
The Affiliated Hospital of Xuzhou Medical University
NOT_YET_RECRUITING

Xuzhou, Jiangsu, 221004, China
The First Affiliated Hospital Of Henan University of Science and Technology
NOT_YET_RECRUITING

Luoyang, Henan, 471000, China
The First Affiliated Hospital Of Wannan Medical College
NOT_YET_RECRUITING

Wuhu, Anhui, 241001, China
The First Affiliated Hospital Of Xi 'an Jiaotong University
NOT_YET_RECRUITING

Xi'an, Shaanxi, 710061, China
The First Affiliated Hospital Of Xiamen University
NOT_YET_RECRUITING

Xiamen, Fujian, 361003, China
The First Affiliated Hospital Zhejiang University School of Medicine
NOT_YET_RECRUITING

Hangzhou, Zhejiang, 310016, China
The First Affiliated Hospital of China Medical University
NOT_YET_RECRUITING

Shenyang, Liaoning, 110801, China
The First Affiliated Hospital of Chongqing Medical University
NOT_YET_RECRUITING

Chongqing, Chongqing Municipality, 400010, China
The First Affiliated Hospital of Guangzhou Medical University
NOT_YET_RECRUITING

Guangzhou, Guangdong, 510030, China
The First Affiliated Hospital of Soochow University
NOT_YET_RECRUITING

Suzhou, Jiangsu, 215006, China
The First Affiliated Hospital of Xinjiang Medical University
NOT_YET_RECRUITING

Ürümqi, Xinjiang, 830000, China
The First Affiliated Hospital of Zhengzhou University
NOT_YET_RECRUITING

Zhengzhou, Henan, 450000, China
The First Hospital of Lanzhou University
NOT_YET_RECRUITING

Lanzhou, Gansu, 730000, China
The First People's Hospital Of Changzhou
NOT_YET_RECRUITING

Changzhou, Jiangsu, 213000, China
The First affiliated Hospital of Nanyang Medical College
NOT_YET_RECRUITING

Nanyang, Henan, 474450, China
The Fourth Affiliated Hospital Of Soochow University (SuZhou Du Shu Lake Hospital)
NOT_YET_RECRUITING

Suzhou, Jiangsu, 215124, China
The Fourth Hospital of Hebei Medical University
NOT_YET_RECRUITING

Shijiazhuang, Hebei, 050035, China
The People's Hospital of Guizhou Province
NOT_YET_RECRUITING

Guiyang, Guizhou, 550002, China
The Second Affiliated Hospital Of Nangchang University
NOT_YET_RECRUITING

Nanchang, Jiangxi, 330006, China
The Second Affiliated Hospital Of Zunyi Medical University
NOT_YET_RECRUITING

Zunyi, Guizhou, 550002, China
The Second Affiliated Hospital Zhejiang University School of Medicine
NOT_YET_RECRUITING

Hangzhou, Zhejiang, 310017, China
The Second Affiliated Hospital of Hainan Medical University
NOT_YET_RECRUITING

Haikou, Hainan, 570311, China
The Second Affiliated Hospital of PLA Air Force Military Medical University
NOT_YET_RECRUITING

Xi'an, Shaanxi, 710038, China
The Second Hospital Of Anhui Medical University
NOT_YET_RECRUITING

Hefei, Anhui, 230601, China
The Sixth Affiliated Hospital,Sun Yat-sen University
NOT_YET_RECRUITING

Guangzhou, Guangdong, 510655, China
The first hospital of Jilin University
NOT_YET_RECRUITING

Changchun, Jilin, 130000, China
Tianjin Medical University Cancer Institute & Hospital
NOT_YET_RECRUITING

Tianjin, Tianjin Municipality, 300300, China
Tongji Hospital Tongji Medical College Of Hust
NOT_YET_RECRUITING

Wuhan, Hubei, 430030, China
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
NOT_YET_RECRUITING

Wuhan, Hubei, 433000, China
Weifang Yidu Central Hospital
NOT_YET_RECRUITING

Weifang, Shandong, 262500, China
Wenzhou Medical University Affiliated First Hospital
NOT_YET_RECRUITING

Wenzhou, Zhejiang, 325000, China
West China Hospital,Sichuan University
NOT_YET_RECRUITING

Chengdu, Sichuan, 610041, China
Xijing Hospital
NOT_YET_RECRUITING

Xi'an, Shaanxi, 710032, China
Xuzhou central hospital
NOT_YET_RECRUITING

Xuzhou, Jiangsu, 221000, China
Yuncheng Central Hospital
NOT_YET_RECRUITING

Yuncheng, Shanxi, 044000, China
Yunnan Cancer Hospital
NOT_YET_RECRUITING

Kunming, Yunnan, 650000, China
ZhongShan Hospital
NOT_YET_RECRUITING

Shanghai, Shanghai Municipality, 200030, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.