Prospective Research Assessment in Multiple Myeloma: An Observational Evaluation (PREAMBLE)

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria:

For RRMM participants who have received at least one prior line of therapy (LoT) for MM:

• Have documented progression from a prior LoT

• Participants who have initiated treatment with one of the following therapies within 90 days before consent for this study OR in the case where treatment has not yetbeen initiated, documentation that the treatment strategy was determined beforeconsent for this study must be provided, and treatment must be initiated within 30days after consent:

• IMiDs

• PIs

• Combination of IMiD + PI

• Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Aktinhibitors, SINE, or CAR T-cell therapies)

For NDMM participants receiving frontline therapy:

• Eligible to receive frontline therapy for MM (no prior MM treatment)

• Participants who have initiated treatment for MM with one of the following therapieswithin 90 days before consent for this study OR in the case where treatment has notyet been initiated, documentation that the treatment strategy was determined beforeconsent for this study must be provided, and treatment must be initiated within 30days after consent:

• IMiDs

• PIs

• Combination of IMiD + PI

• Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Aktinhibitors, SINE, or CAR T-cell therapies)

Exclusion Criteria:

• Participants who are currently participating in a clinical trial for MM

• Participants who are currently receiving treatment for primary cancer other than MM

• Participants who are not willing or able to provide informed consent

• Participants who are incarcerated

• Participants under compulsory detention for treatment of a physical (eg, infectious)or psychiatric illness

Other protocol-defined inclusion/exclusion criteria apply