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CC-4047 (Pomalidomide) for Graft vs. Host Disease

2016년 1월 28일 업데이트: Washington University School of Medicine

A Phase 2, Open-Label, Single-Arm, Pilot Study of Safety and Efficacy of CC-4047 (Pomalidomide) in Patients With Advanced Chronic Graft-Versus-Host Disease Developing After Allogeneic Hematological Stem Cell Transplantation

This study will test the safety and effectiveness CC-4047 (pomalidomide) in patients with advanced, steroid refractory graft-versus-host disease.

연구 개요

상태

완전한

개입 / 치료

상세 설명

Chronic Graft vs. Host Disease is a major complication after allogeneic hematopoietic stem cell transplantation developing in 30 - 70% of patients. It is a multisystem alloimmune and autoimmune disorder with a negative impact on quality of life and functional status, increased need for extended immunosuppression and is the leading cause of late transplant related mortality.

CC-4047 is a novel immune modulatory drug that is a thalidomide analog with a 4,000 fold greater inhibition of TNF-α production related to thalidomide. Several features of CC-4047 suggest that this drug may be useful in treating chronic GVHD including in vitro suppression of TNF-α production, increasing Th1 and stimulation of IL-12 and sIL-Rα.

This study is an open-label, single-arm, pilot study of efficacy and safety of CC-4047 in patients with advanced chronic GvHD who failed to achieve a response with high-dose corticosteroids or second line systemic immunosuppressive therapy.

연구 유형

중재적

등록 (실제)

13

단계

  • 2 단계

연락처 및 위치

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

연구 장소

    • Missouri
      • St. Louis, Missouri, 미국, 63122
        • Washington University School of Medicine

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 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Patient must meet all of the following inclusion criteria:

  • Must be greater than or equal to 18 years of age at the time of consent.
  • Must be able to adhere to the study visit schedule and other protocol requirements.
  • Chronic graft versus host disease (GHVD) developing after allogeneic hematological stem cell transplantation diagnosed using NIH criteria for diagnosis and staging of chronic GvHD (including both "classic chronic GvHD" and "overlap syndrome")
  • Must have moderate or severe chronic GvHD according to Global Staging System for Chronic GvHD or mild chronic GvHD with platelet count less than 100 x 109/L
  • Must have failed to achieve response to high dose corticosteroid (average 0.5 mg/kg/day prednisone or equivalent for greater than or equal to 8 weeks), or have failed second line systemic immunosuppressive therapy.
  • If taking corticosteroids at the time of enrollment, must be on stable or tapering schedule without corticosteroid pulses in the preceding 8 weeks.
  • If taking secondary systemic immunosuppressive therapy at the time of enrolment, must be on stable or tapering schedule in the preceding 4 weeks.
  • Karnofsky performance score (KPS) greater than or equal to 60%.
  • Life expectancy greater than or equal to 3 months.
  • Female of childbearing potential (FCBP) must agree to use two reliable forms of contraception simultaneously or to practice complete abstinence from heterosexual intercourse for at least 28 days before starting study drug, while participating in the study, and for at least 28 days after discontinuation from the study. The two methods of reliable contraception must include one highly effective method (i.e. intrauterine device (IUD), hormonal [birth control pills, injections, or implants], tubal ligation, partner's vasectomy) and one additional effective (barrier) method (i.e. latex condom, diaphragm, cervical cap). FCBP must be referred to a qualified provider of contraceptive methods if needed.
  • FCBP must agree to pregnancy testing and contraceptive counseling every 28 days during the study. FCBP must also refrain from donating blood and/or egg while participating in the study and for at least 28 days after discontinuation from this study
  • FCBP must have two negative pregnancy tests (sensitivity of at least 25 mIU/mL) prior to starting study drug. The first pregnancy test must be performed within 10-14 days prior to the start of study drug and the second pregnancy test must be performed within 24 hours prior to the start of study drug.
  • Must agree to abstain from breastfeeding during study participation and for at least 28 days after study drug discontinuation.
  • Male Subjects must agree to complete abstinence or to use a condom during sexual contact with with a pregnant female or a female of childbearing potential while participating in the study and for at least 90 days following study drug discontinuation even if he has undergone a successful vasectomy
  • Must agree to counseling about sexual contact and the potential risks of fetal exposure to pomalidomide every 28 days.
  • Male subjects will be warned that sharing study drug is prohibited
  • Must agree to abstain from donating blood for at least 28 days following discontinuation of the study drug.
  • Must agree to abstain from donating semen or sperm during study participation and for at least 90 days after study drug discontinuation.
  • Must agree that if a pregnancy or a positive pregnancy test does occur in a the partner of a male study subject during study participation, the investigator must be notified immediately
  • Patients must agree to not share study drug with anyone during participation in the study.
  • Must understand and voluntarily sign an informed consent form, or must have a legally authorized representative who is able and willing to voluntarily sign an informed consent form on behalf of the patient.

Exclusion Criteria:

  • Pregnant or lactating females.
  • New immunosuppressive therapy started within the preceding 4 weeks.
  • Extracorporeal photopheresis within the preceding 3 months.
  • Hypersensitivity to any immune modulator drug (IMiD™).
  • Unable to take prophylactic anticoagulation.
  • Any condition which places the patient at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.
  • Acute, persistent, recurrent or late-onset acute GvHD defined by NIH criteria.
  • Any of the following laboratory values at registration:

    • absolute neutrophil count (ANC) less than 1.0 x 109/L,
    • platelets less than 75 x 109/L, or
    • creatinine clearance less than 50 mL/min (Cockroft-Gault formula).
  • Uncontrolled infection requiring systemic antibiotics.
  • Known human immunodeficiency virus (HIV), hepatitis B virus (HBV) and/or hepatitis C virus (HCV) infection.
  • Known uncontrolled arrhythmias or symptomatic heart disease or left ventricular ejection fraction less than 40% (an ECHO should be performed as clinically indicated)
  • Recurrence of cancer for which the transplant was done except for presence of minimal residual disease by PCR.
  • Other cancer less than or equal to 2 years prior study-entry except:
  • Basal cell carcinoma of the skin,
  • Squamous cell carcinoma of the skin,
  • Carcinoma in situ of the cervix,
  • Carcinoma in situ of the breast, or
  • Prostate cancer (Tumor, Node, Metastasis [TNM] stage T1a or T1b)

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: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: CC-4047 Arm
CC-4047 2 mg orally every day for 1 course (12 weeks or 84 days). Every 28 days of treatment are considered as 1 cycle and every 3 cycles are are considered as 1 course of treatment. A total of 4 courses of treatment are planned (12 months).
다른 이름들:
  • 포말리도마이드

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Overall Response (Complete Response + Partial Response + Other)
기간: 1 year after last dose of CC-4047
  • CR is defined as complete resolution in all of signs and symptoms at all affected organs and tissues
  • PR is defined as improvement in greater than or equal to 1 organ/tissue with no progression in any other affected organ/tissue
  • Improvement in chronic GvHD symptoms less than what meets the definition of a PR is defined as other
  • Progressive disease is defined as failure of therapy to control chronic GvHD despite increasing the dose of primary therapy or adding second line treatments
  • No response is defined as no change in disease.
1 year after last dose of CC-4047

2차 결과 측정

결과 측정
측정값 설명
기간
Safety as Measured by the Most Common Adverse Effects and Reasons for Dose Reductions or Study-discontinuation
기간: 30 days after last dose of CC-4047 or until resolution of event
-Toxicities will be graded according to the NCI CTCAE v3.0.
30 days after last dose of CC-4047 or until resolution of event

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: John F. DiPersio, M.D., Ph.D., Washington Univerisity School of Medicine

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

2009년 2월 1일

기본 완료 (실제)

2010년 10월 1일

연구 완료 (실제)

2011년 10월 1일

연구 등록 날짜

최초 제출

2008년 10월 7일

QC 기준을 충족하는 최초 제출

2008년 10월 8일

처음 게시됨 (추정)

2008년 10월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2016년 2월 25일

QC 기준을 충족하는 마지막 업데이트 제출

2016년 1월 28일

마지막으로 확인됨

2016년 1월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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