For Healthcare Professionals

A Phase III, Safety, Tolerability and Efficacy of Combination Treatment of BL-8040 and G-GSF as Compared to Placebo and G-CSF for thE MobilizatioN of HematopoiEtic Stem Cells for Autologous TransplantatIon in SubjectS With MM

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About the study

A total of 207 subjects will be randomized into the study which will employ a double-blind placebo-controlled setting to assess the efficacy and safety of G-CSF + BL-8040 as compared to G-CSF + placebo.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

  1. Histologically confirmed Multiple Myeloma prior to enrolment and randomization.
  2. At least 1 weeks (7 days) from last induction cycle of combination/multi-agent cyto-reductive chemotherapy and no single agent chemotherapy/maintenance within 7 days (e.g. lenalidomide, pomalidomide, bortezomib, dexamethasone, etc).
  3. Eligible for Autologous Hematopoietic stem cell transplantation according at the investigator discretion.
  4. The subjects should be in first or second CR (including CR and SCR) or PR (including PR and VGPR)
  5. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
  6. Adequate organ function at screening .
  7. Subjects must use effective contraception.

EXCLUSION CRITERIA

  1. Previous history of autologous or allogeneic-HCT
  2. Failed previous HSC collections or collection attempts.
  3. Patients whose apheresis product were to be further selected and purified
  4. Taken any of the listed below concomitant medications, growth factors or stimulating agents within the designated washout period:
  5. Dexamethasone: 7 days
  6. Thalidomide: 7 days
  7. Lenalidomide: 7 days
  8. Pamolidomide: 7 days
  9. Bortezomib: 7 days
  10. Carfilzomib: 7 days
  11. G-CSF: 14 days
  12. GM-CSF or Neulasta®: 21 days
  13. Combination/multi-agent cyto-reductive therapy
  14. Erythropoietin or erythrocyte stimulating agents: 30 days
  15. Eltrombopag, romiplostim or platelet stimulating agents: 30 days
  16. Carmustine (BCNU): 42 days/6 weeks l. Daratumumab: 28 days m. Ixazomib: 7 days
  17. Received >6 cycles lifetime exposure to Lenalidomide.
  18. Received >8 cycles of alkylating agent combinations.
  19. Received > 6 cycles of melphalan
  20. Received 3-bis(2-chloroethyl)-1nitrl.
  21. Received prior treatment with radioimmunotherapy, (e.g. radionuclides, holmium).
  22. Received marrow stimulating factors:
  23. Received G-CSF within 14 days prior to anticipated first dose of G-CSF.
  24. Received Pegfilgrastim (GM-CSF or Nulesta) within 3 weeks prior to anticipated first dose of G-CSF.
  25. Received erythrocyte of platelet stimulating agents within 30 days prior to anticipated first dose of G-CSF
  26. Plans to receive maintenance treatment within 60 days post-engraftment (e.g. Lenalidomide, Bortezomib, Pomalidomide, Thalidomide, Carfilzomib, etc.)
  27. Has received a live vaccine within 30 days of the planned start of study therapy. Seasonal flu vaccines that do not contain live virus are permitted.
  28. Known active CNS metastases or carcinomatous meningitis.
  29. A history of allergic reactions attributed to compounds of similar chemical or biologic composition to BL-8040, G-CSF, or other agents used in the study.
  30. Has an active infection requiring systemic therapy or uncontrolled infection. Has a known additional malignancy that is progressing or requires active treatment. Has an underlying medical condition that would preclude study participation.
  31. Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.
  32. O2 saturation < 92% (on room air).
  33. History of unexplained syncope, syncope from an uncorrected cardiac etiology, or family history of sudden death.
  34. History or family history of Long QT Syndrome or Torsade de Pointes. Myocardial infarction, CABG, coronary or cerebral artery stenting and /or angioplasty, stroke, cardiac surgery, or hospitalization for congestive heart failure within 3 months or greater than Class 2 Angina Pectoris or NYHA Heart Failure Class >2. QTcF > 470 msec, PR > 280 msec, Mobitz II 2nd degree AV Block, 2:1 AV Block, High Grade AV Block, or Complete Heart Block, unless the patient has an implanted pacemaker or implantable cardiac defibrillator (ICD) with backup pacing capabilities.
  35. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
  36. Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 30 days after the last dose of trial treatment.
  37. Has a known history of HIV (HIV 1/2 antibodies), active / chronic Hepatitis B or C.
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +972-8-642-9100Email iconEmail Study Center

Study’s details


Contition

Multiple Myeloma

Age

18+

Phase

Phase 3

Participants needed

136

Est. Completion Date

Dec 2025

Treatment type

Interventional


Sponsor

BioLineRx, Ltd.

ClinicalTrials.gov identifier

NCT03246529

Study number

BL-8040.SCM.301

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