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2.6 Patients 2.6.1 Patient selection and study design Patients were enrolled in a prospective, investigator-initiated, non-randomized, multicenter, open-label study designed to evaluate in part A the safety and efficacy of DARA monotherapy in individuals with relapsed/refractory MM (RRMM) ( PB and BM samples from patients treated with DARA monotherapy in part A of the clinical study were collected at baseline, prior to initiation of DARA monotherapy, and at the time of DARA treatment failure (defined as disease progression [PD] during the first cycle of treatment, less than minimal response after the second treatment cycle, or less than partial response [PR] after the third treatment cycle), or in case of PD after an initial response (PR or better) for evaluation of adenosine (ADO) and inosine (INO) levels

Cultures were grown until logarithmic growth in 35 ml 7H9-0.05% Tween-80-ADC supplemented with or without AdoCbl

Treatment time is 15 minutes total (10 minutes for consultation and consent forms)

Impact of statin therapy on plasma levels of plasminogen activator inhibitor-1

Is AOD 9604 Safe

How might BPC 157 affect recovery from exercise or muscle repair