MedPath

An expanded treatment protocol of panobinostat in combination therapy for relapsed and relapsed and refractory (RR) cancer of plasma cells.

Phase 1
Active, not recruiting
Conditions
Multiple myeloma
Therapeutic area: Diseases [C] - Cancer [C04]
MedDRA version: 19.0Level: LLTClassification code 10028228Term: Multiple myelomaSystem Organ Class: 100000004864
Registration Number
EUCTR2014-003239-21-DE
Lead Sponsor
ovartis Pharma Services AG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

- Patient with diagnosis of multiple myeloma, based on IMWG definitions, that is relapsed or relapsed and refractory to at least two prior regimens including bortezomib and an immunomodulatory agent.
a. Relapsed, defined by disease that recurred in a patient that responded under at least two prior regimens including bortezomib and an immunomodulatory agent, by reaching a MR or better, and had not progressed under current therapy or up to 60 days of last dose of this therapy. Patients previously treated with bortezomib are eligible.
b. Relapsed-and-refractory to a therapy, provided that patient meets both conditions:
•patient has relapsed to at least two prior regimens including bortezomib and an immunomodulatory agent
•and patient was refractory to at least two prior regimens including bortezomib and an immunomodulatory agent by either not reaching a MR, or progressed while under this therapy, or within 60 days of its last
dose. Patients previously treated with bortezomib are eligible even if they are deemed refractory.

- Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of = 2
- Absolute neutrophil count (ANC) = 1.0 x 109 /L
- Platelet count = 100 x 109 /L

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 75
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 125

Exclusion Criteria

- Patient has shown intolerance or has any contraindications to bortezomib, dexamethasone or panobinostat
- Patient is refractory to panobinostat
- Patient has grade = 2 peripheral neuropathy
- Patient taking any anti-cancer therapy concomitantly (bisphosphonates are permitted)
- Patient requires medication with a risk of prolonging the QT interval or inducing Torsades de pointes

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.