Trials / Enrolling By Invitation
Enrolling By InvitationNCT04491721
Follow-up the OS and PFS of Rituximab Biosimilar HLX01 and MabThera, in Untreated Subjects With CD20+ DLBCL
Long-term Follow-up the OS and PFS of Rituximab Biosimilar HLX01 and MabThera in Combination With CHOP, in Previously Untreated Subjects With CD20+ DLBCL
- Status
- Enrolling By Invitation
- Phase
- —
- Study type
- Observational
- Enrollment
- 407 (estimated)
- Sponsor
- Chinese Academy of Medical Sciences · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The main objective of this study is to observe the overall survival of Rituximab Biosimilar HLX01 and MabThera in Combination With CHOP, in previously untreated subjects with CD20+ DLBCL. The secondary objective of this study is to observe the progression-free survival of Rituximab Biosimilar HLX01 and MabThera in Combination With CHOP, in previously untreated subjects with CD20+ DLBCL.
Detailed description
1. Enrollment:407 subjects. 2. The inclusion criteria of this study: subjects who have participated in Phase III clinical trials.Phase III clinical trial(NCT02787239) has ended. 3. The exclusion criteria: ①Subjects died; ②Subjects are unwilling to participate in follow-up study; ③ the investigator judges that the subject is not suitable for participating the study. 4. Duration and method of follow-up: 2-10 years (2020-2027)after the end of the Phase III trial and follow up the subjects by the phone. 5. Statistical analysis method: For progression-free survival and overall survival (OS), the median time and its 95% confidence intervals will be calculated by the Kaplan-Meier method.The Log-Rank test will be used for finding the difference between groups. The efficacy will be analyzed by SAS9.4 , and all hypothesis tests are two-sided. The confidence level of all confidence intervals is 95%. P value less than 0.05 was regarded as statistically significant.
Conditions
Timeline
- Start date
- 2020-07-01
- Primary completion
- 2027-06-01
- Completion
- 2027-07-01
- First posted
- 2020-07-29
- Last updated
- 2020-07-29
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04491721. Inclusion in this directory is not an endorsement.