All regulations
Nonrulemaking
FDA
Open for Comments
FDA-2025-D-2616
Minimal Residual Disease and Complete Response in Multiple Myeloma: Use as Endpoints to Support Accelerated Approval; Draft Guidance for Industry; Availability
Documents
2
Comments
21
Key Dates
Comment Period OpensJan 21, 2026
Comment Period ClosesMar 24, 2026
Documents
Comment Statistics
Total Comments
21
Keywords
2024-798
CDRH
CBER
CDER
Minimal Residual Disease and
Complete Response in Multiple Myeloma Use as
Endpoints to Support Accelerated Approval
Draft Guidance for Industry Availability
Data from Regulations.gov