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1. Adaptive designs for clinical trials of drugs and biologics

3. Antibiotics: FDA has encouraged development, but needs to clarify the role of draft guidance and develop qualified infectious disease product guidance : report to Congressional requesters

6. COVID-19 public health emergency: general considerations for pre-IND meeting requests for COVID-19 related drugs and biological products : guidance for industry and investigators

7. Chemistry, manufacturing, and control (CMC) information for human gene therapy investigational new drug applications (INDs)

8. Clinical drug interaction studies: cytochrome P450 enzyme- and transporter-mediated drug interactions

10. Duchenne muscular dystrophy and related dystrophinopathies: developing drugs for treatment