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Safety and Efficacy of Intravenous Autologous Mesenchymal Stem Cells for MS: a Phase 2 Proof of Concept Study (MESCAMS)

2020년 3월 3일 업데이트: Ottawa Hospital Research Institute

MEsenchymal Stem Cell Therapy for CAnadian MS Patients

The mechanism of action of MSC relies on their ability to modulate pathogenic immune responses and provide neuroprotection through the release of anti-apoptotic, anti-oxidant and trophic factors as demonstrated by in-vitro and in-vivo preclinical studies.

Patients will be randomized to receive immediate vs. delayed treatment with either a dose equal to 1-2 millions/kg of body weight of autologous MSC, or equivalent volume of suspension media at baseline. At week 24 treatments will be reversed.

The primary outcome of this study is to evaluate:

  • Treatment's safety within one year from MSC administration by measuring the number, time-frame and severity of adverse events and
  • Treatment's activity in terms of reduction in total number of gadolinium-enhancing lesions (GEL) by magnetic resonance imaging (MRI) scans.

Secondary outcomes are to gain preliminary information on the efficacy of the experimental treatment in terms of combined MRI activity and clinical efficacy (incidence of relapses and disability progression).

연구 개요

상태

완전한

상세 설명

The mechanism of action of Mesenchymal Stem Cells (MSCs) relies on their ability to modulate pathogenic immune responses and provide neuroprotection through the release of anti-apoptotic, anti-oxidant and trophic factors as demonstrated by in vitro and in vivo preclinical studies.

Patients will be randomized to receive immediate vs. delayed treatment with either a dose equal to 1-2 millions/kg of body weight of autologous MSC, or equivalent volume of suspension media at baseline. At 6 months treatments will be reversed.

The primary outcome of this study is to evaluate

  • treatment's safety within one year from MSC administration by measuring the the number, time-frame and severity of adverse event and
  • treatment's activity in terms of reduction in the total number of contrast-gadolinium enhancing lesions (GEL) by magnetic resonance imaging (MRI) scans.

Secondary outcomes are to gain preliminary information on the efficacy of the experimental treatment in terms of combined MRI activity and clinical efficacy (incidence of relapses and disability progression).

연구 유형

중재적

등록 (실제)

31

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Manitoba
      • Winnipeg, Manitoba, 캐나다, R3A 1R9
        • Health Sciences Centre
    • Ontario
      • Ottawa, Ontario, 캐나다, K1H 8L6
        • Ottawa Hospital - General Campus

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • 1) Males and females with a diagnosis of MS

    1. Relapsing remitting MS (RRMS) not responding to at least 1 year of attempted therapy with one or more of the approved therapies (beta-interferon, glatiramer acetate, natalizumab, mitoxantrone, fingolimod, dimethyl fumarate, teriflunomide, alemtuzumab) as evidenced by at least one of the following:

      • i) ≥1 clinically documented relapse in past 12 months
      • ii) ≥2 clinically documented relapses in past 24 months
      • iii) ≥1 gadolinium-enhancing lesion (GEL) at MRI performed within the past 12 months
    2. Secondary progressive MS (SPMS) not responding to at least a year of attempted therapy with one or more of the approved therapies (beta-interferon, glatiramer acetate, natalizumab, mitoxantrone, fingolimod, dimethylfumarate, teriflunomide, alemtuzumab) as evidenced by both:

      • i) an increase of ≥1 EDSS point (if at randomization EDSS ≤ 5.0) or 0.5 EDSS point (if at randomization EDSS ≥ 5.5) in the past 12 months
      • ii) ≥1 clinically documented relapse or ≥ 1 gadolinium-enhancing lesion (GEL) at MRI within the past 12 months
    3. Primary progressive MS (PPMS) patients with all the following features:

      • i) an increase of ≥1 EDSS point (if at randomization EDSS ≤ 5.0) or 0.5 EDSS point (if at randomization EDSS ≥5.5), in the past 12 months
      • ii) ≥ 1 gadolinium-enhancing lesion (GEL) at MRI performed within the past 12 months
      • iii) positive cerebrospinal fluid (CSF) (oligoclonal banding)
  • 2) Age 18 to 50 years old, inclusive at time of informed consent
  • 3) Disease duration 2 to 15 years (inclusive)
  • 4) EDSS 2.5 to 6.5
  • 5) Able and willing to sign informed consent prior to any study-related activities

Exclusion Criteria:

  • 1) RRMS not fulfilling inclusion criteria
  • 2) SPMS not fulfilling inclusion criteria
  • 3) PPMS not fulfilling inclusion criteria
  • 4) A history of active or chronic infection including infection with HIV1-2, chronic Hepatitis B or Hepatitis C
  • 5) Treatment with any immunosuppressive therapy, including natalizumab and fingolimod, within the 3 months prior to randomization
  • 6) Previous treatment with cladribine or alemtuzumab
  • 7) Treatment with interferon-beta, glatiramer acetate, teriflunomide or dimethyl fumarate within the 30 days prior to randomization (all teriflunomide patients will be required to have followed a wash-out with either cholestyramine or activated charcoal as indicated in the product monograph)
  • 8) Treatment with corticosteroids within the 30 days prior to randomization
  • 9) Relapse occurred during the 60 days prior to randomization
  • 10) Previous history of a malignancy (patient reported) other than basal cell carcinoma of the skin or carcinoma in situ that has been in remission for more than one year
  • 11) Severely limited life expectancy by any other co-morbid illness
  • 12) History of previous diagnosis of myelodysplasia or previous hematologic disease (patient reported) or current clinically relevant abnormalities of white blood cell counts
  • 13) Pregnancy or risk of pregnancy (this includes participants that are not willing to practice active contraception for the duration of the study)
  • 14) eGFR < 60 mL/min/1.73m2 or known renal failure or inability to undergo MRI examination
  • 15) Known allergy to gentamicin or related aminoglycosides
  • 16) Inability to give written informed consent in accordance with research ethics board guidelines
  • 17) Concomitant participation in another clinical trial
  • 18) Inability to adhere to protocol according to the investigator's medical judgement

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 크로스오버 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Autologous Mesenchymal Stem Cells
At week 0 a single infusion of either ex-vivo expanded autologous MSC or suspension media will be administered intravenously at a dose of 1 to 2 x 1000000 MSC/Kg body weight. At week 24, another infusion will be performed for cross-over re-treatment: at week 24 treatments will be reversed compared to week 0.

Mesenchymal Stem Cells in Plasma-Lyte A (Baxter) suspension media, containing 5% Human Albumin and 10% dimethylsulfoxide (DMSO, total volume of 5mL DMSO in final cell product) and autologous MSCs at a dose of 1 to 2 x 106 MSC/Kg participant's body weight at randomization.

Matching placebo Plasma-Lyte A (Baxter) suspension media, containing 5% Human Albumin and 10% DMSO (total volume of 5mL DMSO in final cell product).

실험적: Suspension media
At week 0 a single infusion of either ex-vivo expanded autologous MSC or suspension media will be administered intravenously at a dose of 1 to 2 x 1000000 MSC/Kg body weight. At week 24, another infusion will be performed for cross-over re-treatment: at week 24 treatments will be reversed compared to week 0.

Mesenchymal Stem Cells in Plasma-Lyte A (Baxter) suspension media, containing 5% Human Albumin and 10% dimethylsulfoxide (DMSO, total volume of 5mL DMSO in final cell product) and autologous MSCs at a dose of 1 to 2 x 106 MSC/Kg participant's body weight at randomization.

Matching placebo Plasma-Lyte A (Baxter) suspension media, containing 5% Human Albumin and 10% DMSO (total volume of 5mL DMSO in final cell product).

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Safety
기간: 24 weeks from first infusion
Incidence and severity of adverse events in MSC treatment group compared to placebo group
24 weeks from first infusion
Efficacy
기간: 24 weeks from first infusion
Total number of gadolinium-enhancing lesions (GEL) on MRI scan
24 weeks from first infusion

2차 결과 측정

결과 측정
측정값 설명
기간
Efficacy
기간: 48 weeks from first infusion
Number of gadolinium-enhancing lesions (GEL) counted over week 28, 36, 48 compared with the number of GEL counted over 4, 12, 24 weeks.
48 weeks from first infusion
Efficacy
기간: 24 weeks from first infusion
Combined unique magnetic resonance imaging (MRI) activity (number of new or enlarging T2, or enhancing or re-enhancing lesions), volume of gadolinium-enhancing lesions (GEL) and volume of black holes (BH) over 4, 12, 24 weeks compared between treatment groups.
24 weeks from first infusion
Efficacy
기간: 48 weeks from first infusion
Combined unique magnetic resonance imaging (MRI) activity, volume of gadolinium-enhancing lesions (GEL) and volume of black holes (BH) over week 28, 36, 48 compared with the same outcomes over 4, 12 and 24 weeks.
48 weeks from first infusion
Efficacy
기간: 48 weeks from first infusion
Number of relapses in MSC treatment group vs. placebo group in the first 24 weeks and after cross-over re-treatment in the two groups.
48 weeks from first infusion
Efficacy
기간: 48 weeks from first infusion
Time to sustained progression of disability and proportion of progression-free patients compared between treatment groups during the first 24 weeks and after cross-over.
48 weeks from first infusion

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Mark S. Freedman, MSc MD FRCPC, Ottawa Hospital Research Institute

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2015년 6월 1일

기본 완료 (실제)

2019년 12월 1일

연구 완료 (실제)

2019년 12월 1일

연구 등록 날짜

최초 제출

2014년 9월 10일

QC 기준을 충족하는 최초 제출

2014년 9월 10일

처음 게시됨 (추정)

2014년 9월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2020년 3월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2020년 3월 3일

마지막으로 확인됨

2020년 3월 1일

추가 정보

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아니

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