Phase II Study of Biaxin, Revlimid, and Dexamethasone for Untreated Multiple Myeloma

Multiple Myeloma Clinical Trial

Official title:

A Phase II Study of Clarithromycin (Biaxin), Lenalidomide (Revlimid), and Dexamethasone (Decadron) for Newly Diagnosed Subjects With Multiple Myeloma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00151203
• Other study ID #: 0409007427
• Status: Completed
• Phase: Phase 2
• Start date: December 2004
• Est. completion date: September 29, 2020

Study information

• Verified date: May 2021
• Source: Weill Medical College of Cornell University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

PRIMARY STUDY OBJECTIVES

• To evaluate the efficacy of the combination of clarithromycin (Biaxin®), lenalidomide (Revlimid™), and dexamethasone (Decadron®) as an induction therapy for patients with newly diagnosed multiple myeloma (MM).

• To evaluate the safety of the combination of clarithromycin, lenalidomide, and dexamethasone as an induction therapy for patients with newly diagnosed MM.

SECONDARY STUDY OBJECTIVES

• To examine the role of clarithromycin on the pharmacokinetic properties of dexamethasone and lenalidomide.

• To examine the angiogenesis profile in untreated patients and in patients receiving induction therapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: September 29, 2020
• Est. primary completion date: April 2007
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subject must voluntarily sign and understand written informed consent.

• Histologically confirmed Durie-Salomon stage II or III MM (see Appendix II). Stage I MM patients will be eligible if they display poor prognostic factors (ß2M > or = 5.5 mg/L, plasma cell proliferation index > or = 5%, albumin of less then 3.0, and unfavorable cytogenetics).

• Measurable disease as defined by > 1.0 g/dL serum monoclonal protein, >0.1 g/dL serum free light chains, > 0.2 g/24 hrs urinary M-protein excretion, and/or measurable plasmacytoma(s).

• Age > or = 18 years at the time of signing the informed consent form.

• Karnofsky performance status > or = 70% (>60% if due to bony involvement of myeloma (see Appendix V).

• No prior treatment or less than one full course of first-line therapy. Patients may be receiving adjuvant antiresorptive therapy (i.e., pamidronate or zoledronic acid) as routine care.

• If the patient is a woman of childbearing age, she must have a negative serum or urine pregnancy test within 7 days of starting study.

• Due to the unknown risk of teratogenic side effects, subjects (women and men) must agree to use effective contraception throughout the duration of the study and for at least 1 month after discontinuation of study drugs.

• Life expectancy > 3 months

• Absolute neutrophil count (ANC)> or = 1000 cells/mm3 (1.0 x 109/L)

• Platelets count > or = 75,000/mm3 (75 x 109/L)

• Serum SGOT/AST < 3.0 x upper limits of normal (ULN)

• Serum SGPT/ALT < 3.0 x upper limits of normal (ULN)

• Serum creatinine < 2.5 mg/dL (221 µmol/L)

• Serum total bilirubin < 2.0 mg/dL (34 µmol/L)

Exclusion Criteria:

• Patients with non-secretory MM (no measurable monoclonal protein, free light chains, and/or M-spike in blood or urine).

• Prior history of other malignancies (except for basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast) unless disease free for ³ 5 years.

• NYHA Class III or IV heart disease. History of active angina, congestive heart disease, or myocardial infarction within 6 months.

• Pregnant or lactating women are ineligible.

• Known HIV positivity

• Active viral or bacterial infections or any coexisting medical problem that would significantly increase the risks of this treatment program.

• Known hypersensitivity to dexamethasone, clarithromycin, lenalidomide, or thalidomide.

• Prior therapy for the treatment of MM

• History of thromboembolic event or other condition currently requiring anticoagulation with warfarin (Coumadin). Patients whose therapy is changed to heparin are eligible.

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• Clarithromycin, Lenalidomide, Dexamethasone
Dexamethasone (Decadron®) will be given orally at a dose of 40 mg on days 1, 2, 3, 8, 15 and 22 during the first cycle and once a week on days 1, 8, 15, and 22 for each subsequent cycle. Clarithromycin (Biaxin®) will be given orally at a dose of 500 mg twice a day beginning on day 2 of cycle 1. Lenalidomide (Revlimid®) will be given orally at a dose of 25 mg daily beginning on day 3 and ending on day 21 of cycle 1 and on days 1-21 of subsequent cycles.

Locations

Country	Name	City	State
United States	Weill Medical College of Cornell University	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Weill Medical College of Cornell University	Celgene Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response rate, time to maximum response, toxicities		3 years