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Clarithromycin in Multiple Myeloma Induction Therapy (CLAIM)

Primary Purpose

Multiple Myeloma

Status
Terminated
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Clarithromycin
Placebo
VCD induction therapy
Sponsored by
Henrik Gregersen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma focused on measuring Multiple Myeloma, Clarithromycin, Induction Chemotherapy, Transplantation, Autologous

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Myeloma diagnosis according to IMWG criteria
  • Treatment demanding disease
  • High-dose melphalan with stem cell support scheduled as a part of the treatment
  • Signed informed consent given prior to any study related activities
  • Age > 18 years

Exclusion Criteria:

  • Allogeneic transplantation scheduled as a part of the treatment
  • Myeloma treatment prior to entry in the study, except radiotherapy, bisphosphonates/denosumab or corticosteroids for symptom control
  • Concurrent disease making clarithromycin treatment unsuitable
  • Positive pregnancy test (only applicable for women with childbearing potential)
  • Known or suspected hypersensitivity or intolerance to clarithromycin
  • Prolonged QT corrected (QTc) interval ( > 500 msec on screening ECG)
  • Concurrent treatment with cabergoline, fluconazole, ketoconazole, pimozide, quetiapine, sirolimus, verapamil, tacrolimus, ergot alkaloid, simvastatin or other statins
  • Uncontrolled or severe cardiovascular disease including myocardial infarction within 6 months of enrolment, uncontrolled angina or known cardiac amyloidosis
  • Severe renal dysfunction (estimated creatinine clearance <10 mL/min)
  • Serious medical or psychiatric illness which, in the judgment of the investigator, would make the patient inappropriate for entry into the study

Sites / Locations

  • Department of Hematology, Aalborg University Hospital
  • Department of Hematology, Aarhus University Hospital
  • Department of Hematology, Rigshospitalet
  • Department of Hematology, Herlev Hospital
  • Department of Hematology, Odense University Hospital
  • Department of Hematology, Roskilde Hospital
  • Department of Hematology, Vejle Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Clarithromycin

Placebo

Arm Description

Clarithromycin combined with VCD induction therapy

Placebo combined with VCD induction therapy

Outcomes

Primary Outcome Measures

Comparison of number of participants with very good partial response or better response after three courses of VCD combined with clarithromycin or placebo

Secondary Outcome Measures

Comparison of number of participants with very good partial response or better response after HDT in patients treated with three courses of VCD combined with clarithromycin or placebo
Comparison of number of participants with sCR, CR, PR, PD or SD in the treatment groups after induction therapy and HDT, respectively
Comparison of frequency of infections in patients treated VCD combined with clarithromycin or placebo
Comparison of number of stem cells harvested in patients treated with clarithromycin and placebo in combination with VCD
Neurotoxicity assessed by FACT/GOG-Ntx, Version 4.0
Quality of life assessed by EORTC QLQ-MY20
Quality of life assessed by EORTC QLQ-C30
Comparison of adverse events in patients treated VCD combined with clarithromycin or placebo assessed by CTCAE v4.0

Full Information

First Posted
October 8, 2015
Last Updated
September 19, 2016
Sponsor
Henrik Gregersen
Collaborators
Danish Myeloma Study Group
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1. Study Identification

Unique Protocol Identification Number
NCT02573935
Brief Title
Clarithromycin in Multiple Myeloma Induction Therapy
Acronym
CLAIM
Official Title
A Randomized Placebo-controlled Phase II Study of Clarithromycin or Placebo Combined With VCD Induction Therapy Prior to High-dose Melphalan With Stem Cell Support in Patients With Newly Diagnosed Multiple Myeloma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Terminated
Why Stopped
Suspected side effects to the combination of clarithromycin and VCD (bortezomib, cyclophosphamide and dexamethasone)
Study Start Date
January 2015 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Henrik Gregersen
Collaborators
Danish Myeloma Study Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the potential synergic anti-myeloma activity of clarithromycin when combined with VCD induction therapy in patients with newly diagnosed multiple myeloma.
Detailed Description
The survival in younger myeloma patients improved in the nineties with the introduction of high-dose melphalan with autologous stem cell support (HDT). However, all patients will eventually experience relapse after HDT and there is a need for improvement of the response after HDT. The choice of induction treatment before HDT affects the outcome after induction therapy as well as the outcome after HDT. Clarithromycin is a macrolide antibiotic frequently utilized in the treatment of respiratory tract infections and is often used in patients with known hypersensitivity to beta-lactam antibiotic. Besides antibiotic activity, clarithromycin may exert immunomodulatory and anti-inflammatory effects. The toxicity profile of clarithromycin is favourable and the cost is very low. Studies on cell lines have shown that clarithromycin attenuates autophagy in myeloma cells and a recent study has demonstrated that treatment with clarithromycin enhanced bortezomib-induced cytotoxicity in myeloma cells. Phase II studies without control groups have indicated that clarithromycin might enhance the effect of the thalidomide and lenalidomide. A case-matched analysis compared patients at one centre receiving clarithromycin, lenalidomide and dexamethasone with an equal number of patients at another centre receiving lenalidomide and dexamethasone. This study indicated a favourable effect of clarithromycin with a higher frequency of complete response, very-good-partial-response or better response and progression-free survival. However, there is a need for controlled studies to determine whether clarithromycin might enhance the effect of other myeloma agents. This randomized placebo-controlled study will include 160 patients with newly diagnosed multiple myeloma eligible for HDT. The study evaluates the potential synergic anti-myeloma activity of clarithromycin when combined with VCD induction therapy in patients with newly diagnosed multiple myeloma, and is conducted by the Danish Myeloma Study Group (DMSG) at seven clinics in Denmark. The first patient was included in May 2015 and enrolment is expected to continue until October 2016. The study ends when the last included patient has been followed for two months after HDT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
Multiple Myeloma, Clarithromycin, Induction Chemotherapy, Transplantation, Autologous

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
58 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clarithromycin
Arm Type
Experimental
Arm Description
Clarithromycin combined with VCD induction therapy
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo combined with VCD induction therapy
Intervention Type
Drug
Intervention Name(s)
Clarithromycin
Intervention Description
p.o. clarithromycin 500 mg twice daily for 63 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablet twice daily for 63 days
Intervention Type
Drug
Intervention Name(s)
VCD induction therapy
Intervention Description
Three courses of VCD (sc bortezomib 1.3 mg/sqm days 1, 4, 8, 11, iv cyclophosphamide 500 mg/sqm on days 1 and 8, and p.o. dexamethasone 40 mg days 1, 2, 4, 5, 8, 9, 11, 12 in each 21-days course)
Primary Outcome Measure Information:
Title
Comparison of number of participants with very good partial response or better response after three courses of VCD combined with clarithromycin or placebo
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Comparison of number of participants with very good partial response or better response after HDT in patients treated with three courses of VCD combined with clarithromycin or placebo
Time Frame
Five months
Title
Comparison of number of participants with sCR, CR, PR, PD or SD in the treatment groups after induction therapy and HDT, respectively
Time Frame
Five months
Title
Comparison of frequency of infections in patients treated VCD combined with clarithromycin or placebo
Time Frame
9 weeks
Title
Comparison of number of stem cells harvested in patients treated with clarithromycin and placebo in combination with VCD
Time Frame
Three months
Title
Neurotoxicity assessed by FACT/GOG-Ntx, Version 4.0
Time Frame
Five months
Title
Quality of life assessed by EORTC QLQ-MY20
Time Frame
Five months
Title
Quality of life assessed by EORTC QLQ-C30
Time Frame
Five months
Title
Comparison of adverse events in patients treated VCD combined with clarithromycin or placebo assessed by CTCAE v4.0
Time Frame
Three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Myeloma diagnosis according to IMWG criteria Treatment demanding disease High-dose melphalan with stem cell support scheduled as a part of the treatment Signed informed consent given prior to any study related activities Age > 18 years Exclusion Criteria: Allogeneic transplantation scheduled as a part of the treatment Myeloma treatment prior to entry in the study, except radiotherapy, bisphosphonates/denosumab or corticosteroids for symptom control Concurrent disease making clarithromycin treatment unsuitable Positive pregnancy test (only applicable for women with childbearing potential) Known or suspected hypersensitivity or intolerance to clarithromycin Prolonged QT corrected (QTc) interval ( > 500 msec on screening ECG) Concurrent treatment with cabergoline, fluconazole, ketoconazole, pimozide, quetiapine, sirolimus, verapamil, tacrolimus, ergot alkaloid, simvastatin or other statins Uncontrolled or severe cardiovascular disease including myocardial infarction within 6 months of enrolment, uncontrolled angina or known cardiac amyloidosis Severe renal dysfunction (estimated creatinine clearance <10 mL/min) Serious medical or psychiatric illness which, in the judgment of the investigator, would make the patient inappropriate for entry into the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Gregersen, MD
Organizational Affiliation
Aalborg University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Hematology, Aalborg University Hospital
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark
Facility Name
Department of Hematology, Aarhus University Hospital
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Facility Name
Department of Hematology, Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Department of Hematology, Herlev Hospital
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
Facility Name
Department of Hematology, Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Department of Hematology, Roskilde Hospital
City
Roskilde
ZIP/Postal Code
4000
Country
Denmark
Facility Name
Department of Hematology, Vejle Hospital
City
Vejle
ZIP/Postal Code
7100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
20645430
Citation
Gay F, Rajkumar SV, Coleman M, Kumar S, Mark T, Dispenzieri A, Pearse R, Gertz MA, Leonard J, Lacy MQ, Chen-Kiang S, Roy V, Jayabalan DS, Lust JA, Witzig TE, Fonseca R, Kyle RA, Greipp PR, Stewart AK, Niesvizky R. Clarithromycin (Biaxin)-lenalidomide-low-dose dexamethasone (BiRd) versus lenalidomide-low-dose dexamethasone (Rd) for newly diagnosed myeloma. Am J Hematol. 2010 Sep;85(9):664-9. doi: 10.1002/ajh.21777.
Results Reference
background
PubMed Identifier
30230047
Citation
Nielsen LK, Klausen TW, Jarden M, Frederiksen H, Vangsted AJ, Do T, Kristensen IB, Frolund UC, Andersen CL, Abildgaard N, Gregersen H. Clarithromycin added to bortezomib-cyclophosphamide-dexamethasone impairs health-related quality of life in multiple myeloma patients. Eur J Haematol. 2019 Jan;102(1):70-78. doi: 10.1111/ejh.13175. Epub 2018 Oct 29.
Results Reference
derived
PubMed Identifier
30123673
Citation
Gregersen H, Do T, Kristensen IB, Frolund UC, Andersen NF, Nielsen LK, Andersen CL, Klausen TW, Vangsted AJ, Abildgaard N. A randomized placebo-controlled phase II study of clarithromycin or placebo combined with VCD induction therapy prior to high-dose melphalan with stem cell support in patients with newly diagnosed multiple myeloma. Exp Hematol Oncol. 2018 Aug 13;7:18. doi: 10.1186/s40164-018-0110-0. eCollection 2018.
Results Reference
derived

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Clarithromycin in Multiple Myeloma Induction Therapy

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