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Spots Global Cancer Trial Database for A Study Comparing Treatment With Lutetium[177Lu] Oxodotreotide Injection to Octreotide LAR in Patients With GEP-NETs

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Trial Identification

Brief Title: A Study Comparing Treatment With Lutetium[177Lu] Oxodotreotide Injection to Octreotide LAR in Patients With GEP-NETs

Official Title: A Study Comparing Treatment With Lutetium[177Lu] Oxodotreotide Injection to Octreotide LAR in Patients With Inoperable, Progressive, , Well Differentiated, Somatostatin Receptor Positive Gastroenteropancreatic Neuroendocrine Tumours

Study ID: NCT05459844

Study Description

Brief Summary: This was a multicenter, stratified, open, randomized, comparator-controlled, parallel-group phase III study comparing treatment with Lutetium\[177Lu\] Oxodotreotide Injection to high dose (60 mg) Octreotide LAR in patients with unresectable or metastatic, progressive, well differentiated (G1 and G2), somatostatin receptor positive gastroenteropancreatic neuroendocrine tumours.

Detailed Description: After the screening period, participants who signed the ICF and were eligible for the study in accordance with the entry criteria were randomly assigned to treatment either Lutetium\[177Lu\] Oxodotreotide Injection or Octreotide LAR. Participant randomization was performed according to a centralized permuted block randomization scheme with a balanced ratio (1:1) between the 2 treatment groups, stratified by primary site of tumor (pancreatic or non-pancreatic), NET pathological grading (G1 or G2) and by the length of time that a participant was on a constant dose of Octreotide (=\< 6 versus \> 6 months). Objective tumor assessment in both groups was performed every 12+/-1 weeks from the randomization date according to RECIST Criteria until progression was centrally confirmed: any participants with progressive disease ceased the treatment/assessment period and proceeded to the long-term follow-up period for evaluation of survival and long-term safety.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Chinese PLA General Hospital, Beijing, Beijing, China

The First Afilliated Hospital of Fujian Medical University, Fuzhou, Fujian, China

The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, China

The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China

The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China

Henan Provincial People's Hospital, Zhengzhou, Henan, China

The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China

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

Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology, Wuhan, Hubei, China

Nanjing First Hospital, Nanjing, Jiangsu, China

The first hospital of Jilin University, Changchun, Jilin, China

The First Affiliated Hospital of AFMU, Xi'an, Shaanxi, China

The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China

Qilu Hospital of Shandong University, Jinan, Shandong, China

Fudan University Shanghai Cancer Center, Shanghai, Shanghai, China

Zhongshan Hospital, Fudan University, Shanghai, Shanghai, China

The First Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, China

West China Hospital of Sichuan University, Chengdu, Sichuan, China

Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China

Mianyang Central Hospital, Mianyang, Sichuan, China

Tianjin Medical University Cancer Institute & Hospital, Tianjin, Tianjin, China

The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China

Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China

Contact Details

Name: Jianming Xu

Affiliation: Chinese PLA General Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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