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Spots Global Cancer Trial Database for A Phase I /IIa Study of RC88-ADC in Subjects With Advanced Malignant Solid Tumors

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Trial Identification

Brief Title: A Phase I /IIa Study of RC88-ADC in Subjects With Advanced Malignant Solid Tumors

Official Title: To Evaluate the Safety of RC88 for Injection in Patients With Advanced Malignant Solid Tumors,Multicenter, Open, Multi-cohort Extension of Efficacy and Pharmacokinetic Characteristics Phase I /IIa Clinical Study

Study ID: NCT04175847

Conditions

Solid Tumor

Interventions

RC88

Study Description

Brief Summary: This was a multicenter, open, multi-cohort extended PHASE I/IIa study, consisting of 2 phases:Phase I (Phase I dose escalation) and Phase II (Phase IIa multi-cohort extension). The objective of this study was to evaluate safety, tolerability, pharmacokinetic characteristics, and initial efficacy in malignant pleural mesothelioma and MSLN in advanced malignant solid tumors.

Detailed Description: Phase I dose escalation phase:This study predicted a total of 6 dose groups, 0.1, 0.5, 1.0, 1.5, 2.0 and 2.5 mg/kg. Phase IIa efficacy exploration phase:This phase is the multi-cohort indication expansion phase. Based on the data obtained in phase I, chose an appropriate dose continue to explore multi-cohort indications, including confirmed malignancy Pleural mesothelioma and MSLN expression were determined.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, Beijing, China

Henan Cancer Hospital, Zhengzhou, Henan, China

Drum Tower Hospital, Nanjing, Jiangsu, China

The First Hospital of Jilin University, Changchun, Jilin, China

The First Hospital of Jilin University, Changchun, Jilin, China

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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