About this trial

This clinical trial is designed to assess the safety, preliminary efficacy, and pharmacokinetics (PK) of DS3790a monotherapy and combination regimens in participants with hematological malignancies.

Eligibility criteria

Qualifiers

Sign and date the ICF, prior to the start of any trial-specific procedures.

Adults >=18 years at the time the ICF is signed.

History of one of the histologically documented hematologic malignancies according to the 5th edition of WHO classification as specified in the protocol.

NHL participants only: Agree to provide baseline tumor tissue samples as specified in the protocol.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • DS3790a
  • Combination drug
  • Combination drug

Treatment groups

420 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.

Locations

5
France
Research Site59037, Lille France
Japan
Research Site464-8681, Nagoya Japan
Research Site104-0045, Tokyo Japan
Research Site135-8550, Tokyo Japan

Sponsors and collaborators

Daiichi Sankyo

Lead sponsor