Safety and Efficacy of TKI258 in Relapsed or Refractory Multiple Myeloma Patients, Who Are With or Without t(4;14) Chromosomal Translocation
This study is ongoing, but not recruiting participants.
Sponsor:
Novartis Pharmaceuticals
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )
ClinicalTrials.gov Identifier:
NCT01058434
First received: January 26, 2010
Last updated: December 5, 2012
Last verified: December 2012
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Purpose
This study will evaluate safety and efficacy of TKI258 in patients with relapsed or refractory multiple myeloma
| Condition | Intervention | Phase |
|---|---|---|
|
Relapsed or Refractory Multiple Myeloma |
Drug: TKI258 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase II, Multi-center, Non-randomized, Open-label Study of TKI258 in Patients With Relapsed or Refractory Multiple Myeloma, Who Are With or Without t(4;14) Translocation |
Resource links provided by NLM:
Further study details as provided by Novartis:
Primary Outcome Measures:
- Overall response rate [ Time Frame: 4 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- frequency and severity of adverse events as per CTCAE [ Time Frame: throughtout the study ] [ Designated as safety issue: No ]
- Progression free survival (PFS) [ Time Frame: every 4 weeks ] [ Designated as safety issue: No ]
- Plasma exposure of TKI258 [ Time Frame: during the first 3 cycles ] [ Designated as safety issue: No ]
| Enrollment: | 43 |
| Study Start Date: | May 2010 |
| Estimated Study Completion Date: | January 2013 |
| Estimated Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: TKI258 | Drug: TKI258 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Cytopathologically or histologically confirmed diagnosis of multiple myeloma previously requiring systemic treatment.
- Evidence of relapsed or refractory disease as documented from the prior treatment history. (Refractory myeloma is defined as disease that is non-responsive while on salvage therapy, or progresses within 60 days of last therapy. Relapsed myeloma is defined as previously treated myeloma which after a period of being off-therapy requires the initiation of salvage therapy. Detailed definitions provided in the PTS-1)
- Have received at least 2 prior treatment regimens for multiple myeloma including chemotherapy, autologous transplantation, immunotherapy, or other investigational agents. Pre-planned induction, followed by transplant and maintenance should be considered as one regimen.
Presence of measurable disease as defined by at least one of the following;
- Serum M-protein ≥ 1g/dL (measurable disease)
- Urine M-protein ≥ 200mg/24 hours by protein electrophoresis (measurable disease)
Exclusion Criteria:
- Patients with non-secretory, or oligosecretory, multiple myeloma.
- Patients with symptomatic amyloidosis, or with plasma cell leukemia.
- Patients who have received allogeneic stem cell transplantation and who show evidence of active graft-versus-host disease that requires immunosuppressive therapy.
Other protocol-defined inclusion/exclusion criteria may apply
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01058434
Show 30 Study Locations
Show 30 Study LocationsSponsors and Collaborators
Novartis Pharmaceuticals
Investigators
| Study Director: | Novartis Pharmaceuticals | Novartis Pharmaceuticals |
More Information
No publications provided
| Responsible Party: | Novartis ( Novartis Pharmaceuticals ) |
| ClinicalTrials.gov Identifier: | NCT01058434 History of Changes |
| Other Study ID Numbers: | CTKI258A2204, 2009-012417-22 |
| Study First Received: | January 26, 2010 |
| Last Updated: | December 5, 2012 |
| Health Authority: | United States: Food and Drug Administration Canada: Health Canada Australia: National Health and Medical Research Council Germany: Ministry of Health Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) Turkey: Ministry of Health Spain: Ministry of Health |
Keywords provided by Novartis:
|
Multiple myeloma relapsed refractory t(4;14) FGFR3 |
Additional relevant MeSH terms:
|
Multiple Myeloma Neoplasms, Plasma Cell Translocation, Genetic Neoplasms by Histologic Type Neoplasms Hemostatic Disorders Vascular Diseases Cardiovascular Diseases Paraproteinemias |
Blood Protein Disorders Hematologic Diseases Hemorrhagic Disorders Lymphoproliferative Disorders Immunoproliferative Disorders Immune System Diseases Chromosome Aberrations Pathologic Processes |
ClinicalTrials.gov processed this record on May 21, 2013