Tests HMPL-760 with R-GemOx in relapsed or refractory large B-cell lymphoma
Tests HMPL-760 plus R-GemOx against placebo plus R-GemOx in adults with returned lymphoma.
Plain-language title generated from the registry record
Registry title: A Phase III Study of HMPL-760 Plus R-GemOx VS Placebo Plus R-GemOx in Relapsed/Refractory DLBCL
Key facts
- Where
- Baoding, Beijing, Bengbu, Changchun, Changsha, Chengdu, Chongqing, Fujian, Fuzhou, Guangzhou, Guiyang, Hangzhou, Harbin, Hefei, Jinan, Kunming, Nanchang, Nanjing, Nanning, Qingdao, Shanghai, Shenyang, Shenzhen, Taiyuan, Tangshan, Tianjin, Ürümqi, Wenzhou, Wuhan, Xi'an, Xi’an, Xiamen, Xuzhou, and Zhengzhou, ChinaSee the 51 sites
- Phase
- Phase 3
Where in China
- Baoding NO.1 Central HospitalBaoding, ChinaTaking people
- Beijing GoBroad HospitalBeijing, ChinaTaking people
- Beijing Tongren Hospital, Capital Medical UniversityBeijing, ChinaTaking people
- The First Affiliated Hospital of Bengbu Medical CollegeBengbu, ChinaTaking people
- The First Hospital of Jilin UniversityChangchun, ChinaTaking people
- Hunan Cancer HospitalChangsha, ChinaTaking people
- People's Hospital of Hunan ProvinceChangsha, ChinaTaking people
- The Second Xiangya Hospital of Central South UniversityChangsha, ChinaTaking people
- Sichuan Provincial People's HospitalChengdu, ChinaTaking people
- West China Hospital of Sichuan UniversityChengdu, ChinaTaking people
- Chongqing University Cancer HospitalChongqing, ChinaTaking people
- The First Affiliated Hospital of Chongqing Medical UniversityChongqing, ChinaTaking people
- Quanzhou First Hospital.FujianFujian, ChinaTaking people
- Fujian Medical University Union HospitalFuzhou, ChinaTaking people
- Guangdong Provincial People's HospitalGuangzhou, ChinaTaking people
- Sun Yat-sen University Cancer CenterGuangzhou, ChinaTaking people
- ZhuJiang Hospital of Southern Medical University(The Second Clinical Medical College)Guangzhou, ChinaTaking people
- The Affiliated Hospital of Guizhou Medical UniversityGuiyang, ChinaTaking people
- The First Affiliated Hospital, Zhejiang UniversityHangzhou, ChinaTaking people
- Zhejiang Cancer HospitalHangzhou, ChinaTaking people
- Harbin Medical University Cancer HospitalHarbin, ChinaTaking people
- The Second Affiliated Hospital Of Anhui Medical UniversityHefei, ChinaTaking people
- Qilu Hospital of Shandong UniversityJinan, ChinaTaking people
- Shandong Cancer Hospital & instituteJinan, ChinaTaking people
- The First Affiliated Hospital of Kunming Medical UniversityKunming, ChinaNot yet recruiting
- Jiangxi Cancer HospitalNanchang, ChinaTaking people
- Jiangsu Cancer HospitalNanjing, ChinaTaking people
- Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical SchoolNanjing, ChinaTaking people
- The First Affiliated Hospital of Guangxi Medical UniversityNanning, ChinaTaking people
- The Affiliated Hospital of Qingdao UniversityQingdao, ChinaTaking people
- Fudan University Shanghai Cancer CenterShanghai, ChinaTaking people
- Ruijin Hospital Shanghai Jiaotong University School of MedicineShanghai, ChinaTaking people
- Tong Ren Hospital,Shanghai Jiao Tong University School Of MedicineShanghai, ChinaNot yet recruiting
- Tongji Hospital of Tongji UniversityShanghai, ChinaTaking people
- Shengjing Hospital Of China Medical UniversityShenyang, ChinaTaking people
- Shenzhen People's HospitalShenzhen, ChinaTaking people
- Shanxi Provincial Cancer HospitalTaiyuan, ChinaTaking people
- North China University of Science and Technology Affiliated HospitalTangshan, ChinaTaking people
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical CollegeTianjin, ChinaTaking people
- Tianjin Medical University Cancer Institute & HospitalTianjin, ChinaTaking people
- Tianjin People's HospitalTianjin, ChinaTaking people
- People's Hospital of Xinjiang Uygur Autonomous RegionÜrümqi, ChinaTaking people
- The First Affiliated Hospital of WMUWenzhou, ChinaTaking people
- Hubei Cancer HospitalWuhan, ChinaTaking people
- Wuhan Union Hospital of ChinaWuhan, ChinaTaking people
- The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hosiptal)Xi'an, ChinaTaking people
- The First Affiliated Hospital of Xi'an Jiaotong UniversityXi’an, ChinaTaking people
- The First Affiliated hospital of Xiamen UniversityXiamen, ChinaNot yet recruiting
- The affiliated hospital of xuzhou medical universityXuzhou, ChinaTaking people
- Henan Cancer HospitalZhengzhou, ChinaTaking people
- The First Affiliated Hospital of Zhengzhou UniversityZhengzhou, ChinaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Hutchmed
- Trial code
- NCT07409428
- Record updated
- 10 November 2026
- Original description
This is a Phase III randomized, double-blind, positive controlled study to evaluate the efficacy, safety, and pharmacokinetics of HMPL-760 in combination with R-GemOx versus placebo in combination with R-GemOx in patients with R/R DLBCL.Read full original descriptionShow less
A Phase III Randomized, Double-Blind, Positive Controlled Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of HMPL-760 in Combination With R-GemOx Versus Placebo in Combination With R-GemOx in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL)
This is a Phase III randomized, double-blind, positive controlled study to evaluate the efficacy, safety, and pharmacokinetics of HMPL-760 in combination with R-GemOx versus placebo in combination with R-GemOx in patients with R/R DLBCL.
Inclusion: Sign the ICF and be able to follow the requirements of study protocol; Age ≥18 years; ECOG performance status score between 0 and 2; Histopathologically confirmed diagnosis of DLBCL; The investigator judges that the patient's current condition requires further treatment; Patients should have at least one bi-dimensionally measurable lesion; Expected survival is more than 12 weeks.
Exclusion: History of significant organ bleeding, including gastrointestinal bleeding, hematencephalon, haemoptysis, etc., within 8 weeks prior to the first dose of study drug; Known risk of bleeding, such as coagulation factor deficiency, vascular hemophilia; or the patient is receiving vitamin K antagonist (warfarin); The toxic reactions of previous anti-tumor therapy have not recovered to the level of ≤ grade 1 (except for alopecia and decreased appetite and other conditions that have been clearly required in the inclusion and exclusion criteria); Organ insufficiency; Currently known history of liver disease, including cirrhosis, alcoholic liver, known active infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV); Clinically significant active infection; Patients with known primary or secondary central nervous system lymphoma (CNSL) or the presence of clinical symptoms suggestive of CNSL; Women who are pregnant (positive pregnancy test during the screening period) or breastfeeding.