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Study of Carfilzomib in Combination w/Dexamethasone in Patients w/Newly Diagnosed Multiple Myeloma

2017년 10월 23일 업데이트: Jonathan Kaufman, Emory University

An Open-label, Single-arm, Phase 1b/ 2 Study of Carfilzomib in Combination With Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma

The purpose of this study is to evaluate the safety and tolerability of increasing doses of carfilzomib in combination with dexamethasone

연구 개요

연구 유형

중재적

등록 (실제)

1

단계

  • 2 단계

연락처 및 위치

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

연구 장소

    • Georgia
      • Atlanta, Georgia, 미국, 30322
        • Winship Cancer Institute-Emory University

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

Inclusion Criteria:

  • Subjects must have newly diagnosed multiple myeloma immunoglobulin G (IgG), immunoglobulin A (IgA), immunoglobulin E (IgE) or immunoglobulin D (IgD) by the International Myeloma Foundation (IMF) 2003 Diagnostic Criteria
  • Subjects must be treatment naïve.
  • Patient must not have been previously treated with any prior systemic therapy for the treatment of multiple myeloma.
  • Prior treatment of hypercalcemia or spinal cord compression with corticosteroids does not disqualify the patient (the dose should not exceed the equivalent of 160 mg of dexamethasone in a 2 week period).
  • Patients treated with local radiotherapy with or without concomitant exposure to steroids, for pain control or management of cord/nerve root compression, are eligible.
  • One week must have lapsed since last date of radiotherapy, which is recommended to be a limited field.
  • Patients who require concurrent radiotherapy should have entry to the protocol deferred until the radiotherapy is completed and one week have passed since the last date of therapy.
  • Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.
  • All necessary baseline studies for determining eligibility must be obtained within 21 days prior to enrollment.
  • Age 18 years at the time of signing Informed Consent.
  • Life expectancy of more than three months.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2 or Karnofsky performance status of ≥ 60.
  • Subject must be able to adhere to the study visit schedule and other protocol requirements.
  • Written informed consent in accordance with federal, local, and institutional guidelines.
  • Female subjects of child-bearing potential must have a negative serum pregnancy test within seven days of the first dose and agree to use dual methods of contraception during and for 3 months following last dose of drug.
  • Post menopausal females (> 45 years old and without menses for > 1 year) and surgically sterilized females are exempt from a pregnancy test.
  • Male subjects must use an effective barrier method of contraception during study and for three months following the last dose if sexually active with a female of child-bearing potential.
  • Subjects must be able to receive outpatient treatment and laboratory monitoring at the institute that administers agent.

Exclusion Criteria:

  • Patient has > Grade 2 peripheral neuropathy on clinical examination within 14 days before enrollment.
  • Renal insufficiency as measured by calculated creatinine clearance < 15 mL/min by Cockroft-Gault formula.
  • Subjects with evidence of mucosal or internal bleeding and/or platelet refractory (i.e., unable to maintain a platelet count 50,000 cells/mm³).
  • Subjects with an absolute neutrophil count (ANC) < 1000 cells/mm³. Growth factors may not be used to meet ANC eligibility criteria.
  • Total bilirubin > 2.0 mg/dL or bilirubin ≥ 2 x upper limit of normal (ULN).
  • Subjects with a hemoglobin < 8.0 g/dL (Transfusion are permitted).
  • Alanine aminotransferase (ALT) (SGPT) > 2.5 x ULN.
  • Aspartate aminotransferase (AST) ≥ 2.5 x ULN.
  • Major surgery within three weeks of starting study drug (Cycle 1 Day 1).
  • Myocardial infarction within 6 months prior to enrollment or has New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant.
  • Clinically relevant active infection requiring either oral or intravenous antibiotics or antifungal agents.
  • Serious co-morbid medical conditions such as chronic obstructive or chronic restrictive pulmonary disease, and cirrhosis.
  • Any condition, including laboratory abnormalities, that in the opinion of the Investigator places the subject at unacceptable risk if he/she were to participate in the study.
  • Prior malignancy (within the last 3 years) except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, in situ breast cancer, in situ prostate cancer or if the expected survival from other malignancy is less than 90% at 5 years.
  • Uncontrolled diabetes mellitus (Fasting Blood Sugar > 400 despite medical treatment).
  • Known history of POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein (M-protein) and skin changes).
  • Known HIV infection.
  • Known active hepatitis B or C viral infection.
  • Plasma cell leukemia.
  • Glucocorticoid therapy (prednisone > 20 mg/day or equivalent) within the last three weeks.
  • Any prior treatment for multiple myeloma with standard regimens or investigative regimens.
  • Subjects with treatment related myelodysplastic syndrome.
  • Subjects in whom the required program of oral and intravenous fluid hydration is contraindicated, e.g., due to pre-existing significant pulmonary, cardiac or renal impairment.
  • Subjects with known primary amyloidosis.
  • Female subject is pregnant or breast-feeding.
  • Serious medical or psychiatric illness likely to interfere with participation in this clinical study.

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: Carfilzomib in combination with dexamethasone
Carfilzomib will be administered at a dose of 20 mg/m², with a dose escalation to 36 mg/m² after Days 1 and 2 of Cycle 1 in level 1; and at a dose of 20 mg/m², with a dose escalation to 45 mg/m² after Days 1 and 2 of Cycle 1 in level 2 in subjects with multiple myeloma who are newly diagnosed and treatment naïve. Dexamethasone will be given as a fixed dose of 20 mg PO/IV (1, 2, 8, 9, 15, 16, 22, and 23) for cycles 1 to 4 and for subsequent cycles.
다른 이름들:
  • 키프롤리스
다른 이름들:
  • 데카드론

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Tolerability and Safety of Increasing Doses of Carfilzomib in Combination With Dexamethasone.
기간: 24 months
Adverse events will be coded according to the Medical Dictionary for Regulatory Activities (MedDRA) adverse event dictionary. The results will be tabulated to examine their frequency, organ systems affected, and relationship to study treatment. The results of laboratory assessments will be evaluated similarly.
24 months
Patients With ≥ VGPR (Very Good Partial Response)
기간: 4 months-8 months
VGPR will be estimated based on the crude proportion of subjects whose best response is Stringent Complete Response (sCR), Complete Response (CR), and VGPR.
4 months-8 months

2차 결과 측정

결과 측정
측정값 설명
기간
Overall Response Rate (ORR), Defined as sCR, CR, Very Good Partial Response (VGPR), and PR at 4 Cycles
기간: 4 months
The ORR will be estimated based on the crude proportion of subjects for whom best overall response is sCR, CR, VGPR, and PR.
4 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Jonathan Kaufman, MD, Emory University

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

2013년 8월 1일

기본 완료 (실제)

2014년 10월 1일

연구 완료 (실제)

2014년 10월 1일

연구 등록 날짜

최초 제출

2013년 9월 4일

QC 기준을 충족하는 최초 제출

2013년 10월 21일

처음 게시됨 (추정)

2013년 10월 25일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 11월 24일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 10월 23일

마지막으로 확인됨

2017년 10월 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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