A Study of RC48-ADC in Local Advanced or Metastatic Gastric Cancer Subjects With the Overexpression of HER2

Gastric Cancer Clinical Trial

Official title:

A Multicenter, Open Label，Single Arm，Phase II Study to Evaluate the Effect and Safety of Recombinant Humanized Anti-HER2 Monoclonal Antibody-MMAE Conjugate For Injection in HER2 Overexpressing Local Advanced or Metastatic Gastric Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03556345
• Other study ID #: RC48-C008
• Status: Completed
• Phase: Phase 2
• Start date: July 10, 2018
• Est. completion date: August 31, 2020

Study information

• Verified date: January 2022
• Source: RemeGen Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the efficacy and safety of intravenous RC48-ADC in local advanced or metastatic gastric patients with the overexpression of HER2.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 127
• Est. completion date: August 31, 2020
• Est. primary completion date: June 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Voluntary agreement to provide written informed consent.

• Male or female, Age = 18 years and = 80 years.

• Predicted survival = 12 weeks.

• Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.

• All female subjects will be considered to be of child-bearing potential unless they are postmenopausal, or have been sterilized surgically.Female subjects of child-bearing potential must agree to use two forms of highly effective contraception. Male subjects and their female partner who are of child-bearing potential must agree to use two forms of highly effective contraception.

• Willing to adhere to the study visit schedule and the prohibitions and restrictions specified in this protocol.

• Adequate organ function.

• Have had progression or intolerance following receipt of at least two systemic chemotherapy for advanced or metastatic disease.

• HER2 overexpression defined as HER2 IHC 2+ or 3+.

• Measurable disease according to RECIST 1.1.

Exclusion Criteria:

• Known hypersensitivity to Recombinant Humanized Anti-HER2 Monoclonal Antibody-MMAE Conjugate For Injection.

• History of receiving any anti-cancer drug/biologic treatment within 4 weeks prior to trial treatment.

• History of major surgery within 4 weeks of planned start of trial treatment.

• Has received a live virus vaccine within 4 weeks of planned start of trial treatment.

• Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.

• History of other malignancy within the previous 5 years, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, or cancers with a similar curative outcome as those mentioned above.

• Assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol.

Related Conditions & MeSH terms

• Gastric Cancer
• HER2 Overexpressing Gastric Carcinoma
• Stomach Neoplasms

Intervention

Drug:
• RC48-ADC
2.5 mg/kg IV every 2 weeks

Locations

Country	Name	City	State
China	Beijing Cancer Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
RemeGen Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective Response Rate (ORR)	Objective Response Rate was defined as the percentage of participants with a complete response (CR) or partial response (PR)	up to 24 months
Secondary	Progression Free Survival (PFS) as Assessed by investigator	Tumor response was assessed by investigator according to RECIST v1.1	up to 24 months
Secondary	Overall Survival(OS)	OS was defined as the time from the first study treatment to the date of death from any cause	up to 24 months