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N/A N=330

A Survey on NINLARO Risk Management Plan (RMP) Material Utilization Among Pharmacists in Japan

Multiple Myeloma

Enrolled (actual)
330
Serious AEs
Results posted
Jun 2024
Primary outcome: Primary: Number of Pharmacists Who Had Provided Patients With the Contents of the Risk Management Plan (RMP) Material — 307 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
No Intervention (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Takeda
Primary completion
Jun 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Pharmacists Who Had Provided Patients With the Contents of the Risk Management Plan (RMP) Material
307
SECONDARY
Number of Pharmacists Who Had Received the RMP Material for Patients
124
SECONDARY
Number of Pharmacist With Understanding of the Proper NINLARO Dosing Schedule
316
SECONDARY
Number of Pharmacist With Understanding of the Importance of Providing NINLARO Dosing Schedule
298; 30; 1; 1

Summary

This is a survey among pharmacists who have instructed NINLARO therapy in ixazomib, lenalidomide and dexamethasone (IRD) dosing to patients with relapsed/refractory multiple myeloma (rrMM). The main aims of the study are: * To assess the frequency of pharmacists who have provided patients with the contents of the RMP material for patients. * To assess the frequency of pharmacists who have obtained the RMP material for patients. * To evaluate the depth of understanding of proper usage of NINLARO among pharmacists.

Eligibility Criteria

Inclusion criteria

  • Who belong to hospitals prescribing NINLARO.
  • Who have instructed the dosing of NINLARO in IRD therapy to patients.

Exclusion criteria

None

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05882279). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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