CTIS2023-509466-38-00招募中1 期
B9991046 - AVELUMAB MASTER PROTOCOL: AN OPEN-LABEL CONTINUATION STUDY FOR PARTICIPANTS CONTINUING FROM PFIZER-SPONSORED AVELUMAB CLINICAL STUDIES - B9991046
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- Pfizer Inc.
- 入组人数
- 54
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64（—）
- 性别
- All
入选标准
- •1. Any participant who is receiving study treatment and deriving significant clinical benefit (as determined by the Principal Investigator) or is in the safety and/or survival follow-up period in a Pfizer-sponsored Avelumab Parent Study., 2. Participants must agree to follow the reproductive criteria as outlined in Appendix 4 (Section 10.4.1 for males and Section 10.4.2 for females) of the applicable Avelumab Continuation Sub-Study Protocol., 3. Participants who are willing and able to comply with all scheduled visits, treatment plan, and other study procedures as outlined in the appliable Avelumab Continuation Sub- Study Protocol., 4. Capable of giving signed informed consent as described in Appendix 1, Section 10.1.3, which includes compliance with the requirements and restrictions listed in the ICD and in this protocol.
排除标准
- •1. Female participants who are pregnant or breastfeeding., 2. Any medical reason that, in the opinion of the Investigator or Sponsor, precludes the participant from inclusion in the study.
研究者
相似试验
进行中（未招募）
1 期
Master Protocol for Avelumab Continuation StudyEUCTR2021-002457-29-HUPfizer Inc.300
进行中（未招募）
1 期
Master Protocol for Avelumab Continuation StudyThis Master Protocol for Avelumab Continuation Sub-Studies has been designed to accommodate continued access to study intervention, safety follow-up, and when applicable, overall survival follow up, for eligible participants receiving study intervention and who continue to derive treatment benefit or who are in follow-up in a Pfizer-sponsored avelumab study (Parent Study)EUCTR2021-002457-29-DKPfizer Inc.300
进行中（未招募）
1 期
Master Protocol for Avelumab Continuation StudyThis Master Protocol for Avelumab Continuation Sub-Studies has been designed to accommodate continued access to study intervention, safety follow-up, and when applicable, overall survival follow up, for eligible participants receiving study intervention and who continue to derive treatment benefit or who are in follow-up in a Pfizer-sponsored avelumab study (Parent Study)EUCTR2021-002457-29-PLPfizer Inc.300
招募中
3 期
Master Protocol for Avelumab Continuation Study.Cancer2023-509466-38-00Pfizer Inc.14
进行中（未招募）
3 期
Continued Access Study for Participants Deriving Benefit in Pfizer-Sponsored Avelumab Parent Studies That Are ClosingJPRN-jRCT2031210487Kawai Norisuke262