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Relapsing Multiple SclerosisPhase 3BEAT-MSNCT04047628

Best Available Therapy Versus Autologous Hematopoietic Stem Cell Transplant for Multiple Sclerosis (BEAT-MS)

A Phase 3 study testing Autologous Hematopoietic Stem Cell Transplantation and Best Available Therapy (BAT) in people with Relapsing Multiple Sclerosis and Relapsing Remitting Multiple Sclerosis, run by National Institute of Allergy and Infectious Diseases (NIAID) at 23 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

This is a multi-center prospective rater-masked (blinded) randomized controlled trial of 156 participants, comparing the treatment strategy of Autologous Hematopoietic Stem Cell Transplantation (AHSCT) to the treatment strategy of Best Available Therapy (BAT) for treatment-resistant relapsing multiple sclerosis (MS). Read more about this study

Who is it for?
Ages 18 to 55 years
What is being tested?
Autologous Hematopoietic Stem Cell Transplantation and Best Available Therapy (BAT)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
156 participants
Where
23 sitesUnited States
Study dates
17 Aug 2020to 9 Aug 2033
Phase
Phase 3

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 55 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age 18 to 55 years, inclusive, at the time of the screening Visit -2.
  • Diagnosis of MS according to the 2017 McDonald Criteria139.
  • EDSS ≤ 6.0 at the time of randomization (Day 0).
  • T2 abnormalities on brain MRI that fulfill the 2017 McDonald MRI criteria for dissemination in space139. A detailed MRI report or MRI images must be available for review by the site neurology investigator.
  • Highly active treatment-resistant relapsing MS, defined as ≥ 2 episodes of disease activity in the 36 months prior to the screening visit (Visit -2). The two disease activity episodes will be a clinical MS relapse or MRI evidence of MS disease activity and must meet all the criteria described below:
  • At least one episode of disease activity must occur following ≥ 1 month of treatment with one of the following: (i) an oral DMT approved by the FDA for the treatment of relapsing MS, or (ii) a monoclonal antibody approved by the FDA for the treatment of relapsing MS, or (iii) rituximab. Qualifying DMTs include: dimethyl fumarate, diroximel fumarate, monomethyl fumarate, teriflunomide, cladribine, daclizumab, ponesimod, siponimod, ozanimod, fingolimod, rituximab, ocrelizumab, natalizumab, alemtuzumab, ublituximab, and ofatumumab, and
Show all 20Show fewer
  • At least one episode of disease activity must have occurred within the 12 months prior to the screening visit (Visit -2), and
  • At least one episode of disease activity must be a clinical MS relapse (see item c.i. below). The other episode(s) must occur at least one month before or after the onset of the clinical MS relapse, and must be either another clinical MS relapse or MRI evidence of disease activity (see item c.ii. below):
  • Clinical MS relapse must be confirmed by a neurologist's assessment and documented contemporaneously in the medical record. If the clinical MS relapse is not documented in the medical record, it must be approved by the study adjudication committee (see Section 3.5), and ii. MRI evidence of disease activity must include ≥ 1 unique active lesion on one or more brain or spinal cord MRIs. Detailed MRI reports or MRI images must be available for review by the site neurology investigator. A unique active lesion is defined as either of the following:
  • 1. A gadolinium-enhancing lesion, or 2. A new non-enhancing T2 lesion compared to a reference scan obtained not more than 36 months prior to the screening visit (Visit -2).
  • 6. Candidacy for treatment with at least one of the following high efficacy BAT DMTs: cladribine, natalizumab, alemtuzumab, ocrelizumab, ofatumumab, ublituximab and rituximab. Candidacy for treatment for each BAT DMT is defined as meeting all of the following:
  • No prior disease activity episode, as defined in Inclusion Criterion #5, with the candidate BAT DMT, and
  • No contraindication to the candidate BAT DMT, and
  • No treatment with the candidate BAT DMT in the 12 months prior to screening.
  • 7. Completion of COVID-19 vaccination series, according to the current Centers for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP) recommendations, ≥ 14 days prior to randomization (Day 0).
  • 8. Positive for VZV antibodies, or completion of at least one dose of the varicella zoster glycoprotein E (gE) Shingrix vaccine at least 4 weeks prior to randomization (Day 0).
  • 9. Insurance approval for MS treatment with at least one candidate BAT DMT (see Inclusion Criterion #6).
  • 10. Ability to comply with study procedures and provide informed consent, in the opinion of the investigator.
  • 11. Females of childbearing potential (defined in Section 5.4.3.1) and males with female partners of childbearing potential are required to adhere to the contraception provisions of Section 5.4.3.1.
  • 12. For participants who use medicinal or recreational marijuana, willingness to substitute MARINOL® if randomized to AHSCT (Section 5.4.2.6).

Who cannot join

  • Diagnosis of primary progressive MS according to the 2017 McDonald criteria.
  • History of neuromyelitis optica spectrum disorder or MOG antibody disease.
  • Prior treatment with an investigational agent within 3 months or 5 half-lives, whichever is longer. Agents authorized by the FDA for prevention or treatment of COVID-19 are not considered investigational.
  • Either of the following within one month prior to randomization (Day 0):
  • Onset of acute MS relapse, or
  • Treatment with intravenous methylprednisolone 1000 mg/day for 3 days or equivalent.
Show all 44Show fewer
  • Initiation of any BAT DMT (see Section 5.2.1) between Visit -2 and randomization (Day 0).
  • Brain MRI or cerebrospinal fluid (CSF) examination indicating a diagnosis of progressive multifocal leukoencephalopathy (PML).
  • History of cytopenia consistent with the diagnosis of myelodysplastic syndrome (MDS).
  • Presence of unexplained cytopenia, polycythemia, thrombocythemia or leukocytosis.
  • History of sickle cell anemia or other hemoglobinopathy.
  • Evidence of past or current hepatitis B or hepatitis C infection, including treated hepatitis B or hepatitis C. Hepatitis B surface antibody following hepatitis B immunization is not considered to be evidence of past infection.
  • Presence or history of mild to severe cirrhosis.
  • Hepatic disease with the presence of either of the following:
  • Total bilirubin ≥ 1.5 times the upper limit of normal (ULN) or total bilirubin ≥ 3.0 times the ULN in the presence of Gilbert's syndrome, or
  • Alanine Aminotransferase (ALT) or Aspartate Aminotransferase (AST) ≥ 2.0 times the ULN.
  • Positive COVID-19 PCR test, or alternative nucleic acid amplification test (NAAT) per institutional standards, within 14 days prior to randomization (Day 0).
  • Evidence of HIV infection.
  • Positive QuantiFERON - TB Gold,TB Gold Plus, or T-SPOT®.TB test results. PPD tuberculin test may be substituted for QuantiFERON - TB Gold, TB Gold Plus, or T-SPOT®.TB test.
  • Active viral, bacterial, endoparasitic, or opportunistic infections.
  • Active invasive fungal infection.
  • Hospitalization for treatment of infections or parenteral (IV or IM) antibacterials, antivirals, antifungals, or antiparasitic agents within the 30 days prior to randomization (Day 0) unless clearance is obtained from an Infectious Disease specialist.
  • Receipt of live or live-attenuated vaccines within 6 weeks of randomization (Day 0).
  • Presence or history of clinically significant cardiac disease including: a. Arrhythmia requiring treatment with any antiarrhythmia therapy, with the exception of low dose beta blocker for intermittent premature ventricular contractions.
  • Coronary artery disease with a documented diagnosis of either: i. Chronic exertional angina, or ii. Signs or symptoms of congestive heart failure. c. Evidence of heart valve disease, including any of the following: i. Moderate to severe valve stenosis or insufficiency, or ii. Symptomatic mitral valve prolapse, or iii. Presence of prosthetic mitral or aortic valve.
  • Left ventricular ejection fraction (LVEF) < 50%.
  • Impaired renal function defined as eGFR < 60 mL/min/1.73 m2, according to the CKD-EPI formula144.
  • Forced expiratory volume in one second (FEV1) < 70% predicted (no bronchodilator).
  • Diffusing capacity of the lungs for carbon monoxide (DLCO) (corrected for Hgb) < 70% predicted.
  • Poorly controlled diabetes mellitus, defined as HbA1c > 8%.
  • History of malignancy, except adequately treated localized basal cell or squamous skin cancer, or carcinoma in situ of the cervix. Malignancies for which the participant is judged to be cured will be considered on an individual basis by the study adjudication committee (see Section 3.5).
  • Presence or history of any moderate to severe rheumatologic autoimmune disease requiring treatment, including but not limited to the following: systemic lupus erythematous, systemic sclerosis, rheumatoid arthritis, Sjogren's syndrome, polymyositis, dermatomyositis, mixed connective tissue disease, polymyalgia rheumatica, polychondritis, sarcoidosis, vasculitis syndromes, or unspecified collagen vascular disease.
  • Presence of active peptic ulcer disease, defined as endoscopic or radiologic diagnosis of gastric or duodenal ulcer.
  • Prior history of AHSCT.
  • Prior history of solid organ transplantation.
  • Positive pregnancy test or breastfeeding.
  • Failure to willingly accept or comprehend irreversible sterility as a side effect of therapy.
  • Psychiatric illness, mental deficiency, or cognitive dysfunction severe enough to interfere with compliance or informed consent.
  • History of hypersensitivity to rabbit or Escherichia coli-derived proteins.
  • Any metallic material or electronic device in the body, or other condition that precludes the participant from undergoing MRI with gadolinium administration, as determined by the site radiologist.
  • Presence or history of ischemic cerebrovascular disorders, including but not limited to transient ischemic attack, subarachnoid hemorrhage, cerebral thrombosis, cerebral embolism, or cerebral hemorrhage.
  • Presence or history of other neurological disorders, including but not limited to CNS or spinal cord tumor; metabolic or infectious cause of myelopathy; genetically-inherited progressive CNS disorder; CNS sarcoidosis; or systemic autoimmune disorders potentially causing progressive neurologic disease or affecting ability to perform the study assessments.
  • Presence of any medical comorbidity that the investigator determines will significantly increase the risk of treatment mortality.
  • Presence of any other concomitant medical condition that the investigator deems incompatible with trial participation.

Trial locations and contacts

23 sites in 1 country. Contact the study team or a site near you to ask about taking part.

23 sites in 1 country

United States23 sites, 20 recruiting

  • Rocky Mountain Multiple Sclerosis Center, University of Colorado School of Medicine

    Aurora, Colorado, 80045

    Timber Bourassa, BS, 303-724-8305, NeurologyResearchPartners@cuanschutz.edu

    John R. Corboy, MD

    Recruiting

  • University of Virginia

    Charlottesville, Virginia, 22903

    Matthew Baron, 434-297-4102, ukx3sv@uvahealth.org

    Mini Singh, MD

    Recruiting

  • University of Cincinnati (UC) Waddell Center for Multiple Sclerosis

    Cincinnati, Ohio, 45219

    Tiffany Rupert, CCRC, 513-558-0269, BEATMSResearch@UCHealth.com

    Aram Zabeti, MD

    Recruiting

  • Mellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic

    Cleveland, Ohio, 44195

    Alecia Chase, 216-780-4935, chasea@ccf.org

    Jeffrey A. Cohen, MD

    Recruiting

  • University of Texas Southwestern Medical Center: Division of Multiple Sclerosis and Neuroimmunology

    Dallas, Texas, 75390

    Manual Huichapa, 214-645-8216, manuel.huichapa@utsoutwestern.edu

    Benjamin Greenberg, MD

    Recruiting

  • Henry Ford Neuroscience Institute

    Detroit, Michigan, 48202

    Kelly Tundo, kciach1@hfhs.org

    Mirela Cerghet, MD

    Recruiting

  • Duke University Medical Center

    Durham, North Carolina, 27710

    Active, not recruiting

  • Northwestern University

    Evanston, Illinois, 60208

    Matthew Selle, autoimmunesct@nm.org

    George Georges, MD

    Recruiting

  • Maxine Mesigner Multiple Sclerosis Comprehensive Care Center, Baylor College of Medicine Medical Center

    Houston, Texas, 77030

    Tahari Griffin, 713-798-6097, tgriffin@bcm.edu

    George J. Hutton, MD

    Recruiting

  • Medical College of Wisconsin

    Milwaukee, Wisconsin, 53226

    Pam Dailey, 262-689-1846, pdailey@mcw.edu

    Ahmed Obeidat, M.D.

    Recruiting

  • University of Minnesota Multiple Sclerosis Center

    Minneapolis, Minnesota, 55455

    Active, not recruiting

  • Corinne Goldsmith Dickinson Center for Multiple Sclerosis at Mount Siinai

    New York, New York, 10029

    Sarah Myoung, 212-241-3391, sarah.myoung@mssm.edu

    Gena Persad, 212-241-6604

    Recruiting

  • Stanford Multiple Sclerosis Center

    Palo Alto, California, 94304

    Emma Martinez, (650) 387-5907, eam1@stanford.edu

    Jeffrey Dunn, MD, FAAN

    Recruiting

  • Penn Comprehensive MS Center, Hospital of the University of Pennsylvania

    Philadelphia, Pennsylvania, 19104

    MS MS Clinical Research Team, 215-906-4778, msresearch@pennmedicine.upenn.edu

    Amit Bar-Or, MD,FRCP,FAAN,FANA

    Recruiting

  • Multiple Sclerosis Center, Oregon Health & Science University

    Portland, Oregon, 97239

    Debbie Guess, RN, 503-494-7651, griffide@ohsu.edu

    Yadav Vijayshree, MD,MCR,FANA,FAAN

    Recruiting

  • Virginia Commonwealth University Multiple Sclerosis Treatment and Research Center

    Richmond, Virginia, 23219

    Unsong Oh, MD, 804-828-3067, unsong.oh@vcuhealth.org

    Unsong Oh, MD

    Recruiting

  • Mayo Clinic

    Rochester, Minnesota, 55905

    Lisa Roemer, 507-293-9754, Roemer.Lisa@mayo.edu

    B. Mark Keegan, MD,FRCPC

    Recruiting

  • Rochester Multiple Sclerosis Center, University of Rochester

    Rochester, New York, 14620

    Andrew D. Goodman, MD

    Not yet recruiting

  • Clinical Research Division, Fred Hutchinson Cancer Research Center

    Seattle, Washington, 98109

    Active, not recruiting

  • Multiple Sclerosis Center, Swedish Neuroscience Institute

    Seattle, Washington, 98122

    Izzy Bueno, 206-320-4120, Isabella.Bueno1@providence.org

    James D. Bowen, MD

    Recruiting

  • Multiple Sclerosis Center at Northwest Hospital

    Seattle, Washington, 98133

    Elisa McGee, 206-598-9260, emcgee@uw.edu

    Annette Wundes, MD

    Recruiting

  • John L. Trotter Multiple Sclerosis Center, Washington University School of Medicine in St. Louis

    St Louis, Missouri, 63110

    Laura Teeter, 314-747-6247, lteeter@wustl.edu

    Gregory Wu, MD, PhD

    Recruiting

  • University of Massachusetts Memorial Medical Center

    Worcester, Massachusetts, 01655

    Irina Radu, MD, MHA, 774-441-7754, irina.radu@umassmed.edu

    Carolina Ionete, MD, PhD

    Recruiting

Other trials in United States

About this study

Official title: A Multicenter Randomized Controlled Trial of Best Available Therapy Versus Autologous Hematopoietic Stem Cell Transplant for Treatment-Resistant Relapsing Multiple Sclerosis (ITN077AI)

This is a multi-center prospective rater-masked (blinded) randomized controlled trial of 156 participants, comparing the treatment strategy of Autologous Hematopoietic Stem Cell Transplantation (AHSCT) to the treatment strategy of Best Available Therapy (BAT) for treatment-resistant relapsing multiple sclerosis (MS). Participants will be randomized at a 1 to 1 (1:1) ratio.

All participants will be followed for 72 months after randomization (Day 0, Visit 0).

Read the detailed description

Participant recruitment for this six-year research study focuses on multiple sclerosis (MS) that has remained active despite treatment. This study will compare high dose immunosuppression followed by autologous hematopoietic stem cell transplantation (AHSCT) to best available therapy (BAT) in the treatment of relapsing MS.

MS is a disease caused by one's own immune cells. Normally, immune cells fight infection. In MS, immune cells called T cells, or chemical products made by immune cells, react against the covering or coat (myelin) of nerve fibers in the brain and spinal cord. This leads to stripping the coat from certain nerve fibers (demyelination), and this causes neurologic problems. MS can cause loss of vision, weakness or incoordination, loss or changes in sensation, problems with thinking or memory, problems controlling urination, and other disabilities.

Most individuals with MS first have immune attacks (called relapses) followed by periods of stability. Over time, MS can have episodes of new and worsening symptoms, ranging from mild to disabling. This is called relapsing MS. Relapsing MS includes relapsing remitting MS (RRMS) and secondary progressive MS (SPMS). There are medicines (drugs) to decrease relapses, but these are neither considered to be curative nor, to induce prolonged remissions without continuing therapy.

More than a dozen medicines have been approved for the treatment of relapsing forms of MS. These medicines differ in how safe they are and how well they work. Despite availability of an increasing number of effective medicines, some individuals with relapsing MS do not respond to treatment. Research is being conducted to find other treatments.

High dose immunosuppression followed by autologous hematopoietic stem cell transplantation (AHSCT) has been shown to help relapsing MS in cases where medicines did not work. AHSCT involves collecting stem cells, which are produced in the bone marrow. These stem cells are "mobilized" to leave the bone marrow and move into the blood where they can be collected and stored. Participants will then receive chemotherapy intended to kill immune cells. One's own stored (frozen) stem cells are then given back, through an infusion. This "transplant" of one's stem cells allows the body to form new immune cells in order to restore their immune system. New research suggest that MS might be better controlled with AHSCT than with medicines.

Being tested
Autologous Hematopoietic Stem Cell Transplantation, Best Available Therapy (BAT)
Keywords
Treatment-Resistant Relapsing Multiple Sclerosis (MS), Autologous Hematopoietic Stem Cell Transplantation (AHSCT), Autologous Peripheral Blood Stem Cells (PBMCs) Graft, Best Available Therapy (BAT), Disease-Modifying Therapy (DMT), BAT DMT
Medical subject headings
Multiple Sclerosis, Relapsing-Remitting, Multiple Sclerosis, Chronic Progressive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Autologous Hematopoietic Stem Cell TransplantationProcedure or surgery

    Also called AHSCT

    1. PBSC mobilization \& collection regimen per protocol/ institutional standards includes: intravenous cyclophosphamide (Cytoxan®), 4 grams/m^2); intravenous mesna (Mesnex®),a total delivery of 4 grams/m^2); oral dexamethasone, 10 mg dose, four times daily); subcutaneous filgrastim,10 mcg/kg/day until leukapheresis goal is completed; and CD34+ peripheral blood stem cells collection by leukapheresis.
    2. Conditioning per protocol\& institutional standards:
    • 6-day BEAM (e.g. Carmustine (BCNU), Etoposide (VP-16), Cytarbine (Ara-C), and Melphalan) chemotherapy protocol and,
    • rabbit anti-thymocyte globulin (rATG) 2.5 mg/kg/day x2
    1. Autologous cryopreserved graft infusion: The target Cluster of Differentiation (CD)34+ cell dose for infusion is 5 x 10^6 CD34+ cells/kg (minimum 4 x 10^6 CD34+ cells/kg; maximum 7.5 x 10^6 CD34+ cells/kg).

    For 1\&2 above: Ideal body weight (IBW) versus Actual Body Weight (ABW) are applicable.

  • Best Available Therapy (BAT)Biological

    Also called natalizumab (Tysabri®), alemtuzumab (Campath®, Lemtrada®), ocrelizumab (Ocrevus®), rituximab (Rituxan®)

    Disease-modifying therapy (DMT) selected by the Site Investigator from the below:

    • cladribine
    • natalizumab
    • alemtuzumab
    • ocrelizumab,
    • rituximab,
    • ofatumumab, or
    • ublituximab
Study groups in NCT04047628
Study groupRoleWhat they receive
AHSCTExperimentalAHSCT: Myeloablative and Immunoablative therapy followed by Autologous Hematopoietic Stem Cell Transplantation Participants will undergo: 1. Mobilization and graft collection: mobilization of peripheral blood stem cells (PBSC) with cyclophosphamide, filgrastim, and dexamethasone. The autologous graft will be collected by leukapheresis and cryopreserved. 2. Conditioning: high dose myeloablative and immunoablative conditioning with a six-day BEAM chemotherapy and rabbit anti-thymocyte globulin regimen will be initiated ≥30 days after cyclophosphamide mobilization. 3. Autologous cryopreserved graft infusion: the cryopreserved peripheral blood stem cells (PBSC) graft will be thawed and infused the day following completion of the conditioning regimen. Each bag will be thawed and infused according to institutional standards consistent with the Foundation for the Accreditation of Cellular Therapy (FACT) guidelines. Participants will receive prednisone following graft infusion.
Receives: Procedure: Autologous Hematopoietic Stem Cell Transplantation
Best Available Therapy (BAT)Active comparatorParticipants randomized to BAT: Best available therapy will be selected by the Site Investigator from: Cladribine (Mavenclad®), natalizumab (Tysabri®), alemtuzumab (Campath®, Lemtrada®), ocrelizumab (Ocrevus®), ublituximab (BRIUMVI™), rituximab (Rituxan®), or ofatumumab (Arzerra®) (after approval by the FDA for relapsing MS).
Receives: Biological: Best Available Therapy (BAT)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Multiple Sclerosis (MS) Relapse-Free Survival

    MS relapse-free survival, analyzed as time from treatment randomization until MS relapse or death from any cause.

    Measured: From Day 0 (Randomization to Treatment) Up to 36 Months (3 Years)

Secondary outcomes (12)

  1. Number of Multiple Sclerosis (MS) Relapses Per Year

    Annual Relapse Rate (ARR) time calculated as number of confirmed relapses divided by time in study per year.

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  2. The Occurrence of Any Evidence of Multiple Sclerosis (MS) Disease Activity or Death From Any Cause

    The occurrence of any evidence of MS disease activity or death from any cause, analyzed as time-to-event.

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  3. The Occurence of Confirmed Disability Worsening by the Kurtz Expanded Disability Status Scale (EDSS)

    Measured by the Kurtzke Expanded Disability Status Scale performed by the masked (blinded) rater.

    EDSS, defined by:

    • A decrease in EDSS of ≥ 1.0 step(s) compared to the EDSS at randomization (Day 0) and
    • Confirmation of disability improvement ≥ 6 months later. The time of confirmed disability worsening measured by EDSS will be the time of first increase in EDSS ≥ 1.0 step(s).

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  4. The Occurrence of Confirmed Disability Improvement by the Kurtz Expanded Disability Status Scale (EDSS)

    Measured by the Kurtzke Expanded Disability Status Scale performed by the masked (blinded) rater.

    Confirmed disability improvement defined by:

    • A decrease in EDSS of ≥ 1.0 step(s) compared to the EDSS at randomization (Day 0) and
    • Confirmation of disability improvement ≥ 6 months later. The time of confirmed disability improvement measured by EDSS will be the time of first decrease in EDSS ≥ 1.0 step(s).

    Measured: Day 0 (Randomization to Treatment) Up to Month 72 (6 Years)

  5. Whole Brain Volume Change from Pre-Randomization Visit to the follow-up evaluations

    Method of assessment: Magnetic Resonance Imaging (MRI) imaging.

    Measured: From Visit Pre-R Up to 72 Months (6 Years)

  6. Change in Serum Neurofilament Light Chain (NfL) Concentration

    Extent of neurofilament light chain (NfL) concentration in serum is a component of the neuronal cytoskeleton and is released into the cerebrospinal fluid and subsequently blood following neuro-axonal damage.

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  7. The Occurrence of Death From Any Cause: All-Cause Mortality

    Any death, regardless of relationship to treatment.

    Measured: Day 0 (Randomization to Treatment) Up to Month 72 (6 Years)

  8. Proportion of Participants who Experience a Serious Adverse Event (SAE)

    An event that results in any of the following outcomes:

    • Death,
    • A life-threatening event that places the participant at immediate risk of death,
    • Inpatient hospitalization or prolongation of existing hospitalization,
    • Persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, or
    • A congenital anomaly or birth defect.
    • Note: Important medical events that may not result in death, be life threatening, or require hospitalization may be considered serious when, based upon appropriate medical judgment, they may jeopardize the participant and may require medical or surgical intervention to prevent one of the outcomes listed in this definition.

    Reference: Code of Federal Regulations Title 21 Part 312.32(a)

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  9. Proportion of Participants with a Grade 3 or Higher Infection

    In accordance with the criteria set forth in the National Cancer Institute's Common Terminology Criteria for Adverse Events NCI-CTCAE version 5.0, published November 27, 2017.

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  10. Proportion of Participants with Progressive Multifocal Leukoencephalopathy (PML)

    The occurrence of PML during the course of participation in this study.

    A disease of the white matter of the brain, caused by a virus infection, Polyomavirus JC (JC virus), that targets cells that make myelin--the material that insulates nerve cells (neurons).

    Measured: From Day 0 (Randomization to Treatment) Up to 72 Months (6 Years)

  11. Time to Neutrophil Engraftment Among Autologous Hematopoietic Stem Cell Transplantation (AHSCT) Recipients

    Neutrophil engraftment is defined as absolute neutrophil count (ANC) > 500/µl on two consecutive measurements on different days.

    Measured: From Day of Graft Infusion (Receipt of Peripheral Blood Stem Cells-PBSC Infusion) Up to 72 Months (6 Years)

  12. Proportion of Autologous Hematopoietic Stem Cell Transplantation (AHSCT) Recipients Who Experience Primary or Secondary Graft Failure

    Graft failure can either be primary (graft never established) or secondary (loss of an established graft).

    Primary graft failure is the absence of adequate hematopoiesis by Day T28, defined as meeting all of the following conditions:

    • Bone marrow cellularity <5%,
    • Peripheral White Blood Cell Count (WBC) < 500/µl,
    • Peripheral Absolute Neutrophil Count (ANC) < 100/ µl, and
    • Platelets < 10,000/ µl.

    Measured: From Day of Transplant (Receipt of Peripheral Blood Stem Cells-PBSC Infusion) Up to Day 28 Post Transplant

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Aug 2019
  2. Study start17 Aug 2020
  3. Primary completion6 Aug 2030 (estimated)
  4. Study completion9 Aug 2033 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
156 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04047628
Sponsor's protocol ID
DAIT ITN077AI
Other IDs
UM1AI109565, NIAID CRMS ID#: 38573, BMT CTN 1905
Acronym
BEAT-MS
Status last verified
Oct 2026
First submitted
5 Aug 2019
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Participant level data access and additional relevant materials will be made available upon completion of the trial.

Publications

  • Nash RA, Hutton GJ, Racke MK, Popat U, Devine SM, Steinmiller KC, Griffith LM, Muraro PA, Openshaw H, Sayre PH, Stuve O, Arnold DL, Wener MH, Georges GE, Wundes A, Kraft GH, Bowen JD. High-dose immunosuppressive therapy and autologous HCT for relapsing-remitting MS. Neurology. 2017 Feb 28;88(9):842-852. doi: 10.1212/WNL.0000000000003660. Epub 2017 Feb 1.

    PubMed 28148635

  • Nash RA, Hutton GJ, Racke MK, Popat U, Devine SM, Griffith LM, Muraro PA, Openshaw H, Sayre PH, Stuve O, Arnold DL, Spychala ME, McConville KC, Harris KM, Phippard D, Georges GE, Wundes A, Kraft GH, Bowen JD. High-dose immunosuppressive therapy and autologous hematopoietic cell transplantation for relapsing-remitting multiple sclerosis (HALT-MS): a 3-year interim report. JAMA Neurol. 2015 Feb;72(2):159-69. doi: 10.1001/jamaneurol.2014.3780.

    PubMed 25546364

  • Cohen JA, Baldassari LE, Atkins HL, Bowen JD, Bredeson C, Carpenter PA, Corboy JR, Freedman MS, Griffith LM, Lowsky R, Majhail NS, Muraro PA, Nash RA, Pasquini MC, Sarantopoulos S, Savani BN, Storek J, Sullivan KM, Georges GE. Autologous Hematopoietic Cell Transplantation for Treatment-Refractory Relapsing Multiple Sclerosis: Position Statement from the American Society for Blood and Marrow Transplantation. Biol Blood Marrow Transplant. 2019 May;25(5):845-854. doi: 10.1016/j.bbmt.2019.02.014. Epub 2019 Feb 19.

    PubMed 30794930

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