Monocarboxylate Transporter 8 결핍 환자의 Tiratricol에 대한 확장된 액세스 프로그램
Allan-Herndon-Dudley 증후군(AHDS)으로도 알려진 Monocarboxylate Transporter 8 결핍 환자의 Tiratricol에 대한 확장된 액세스 프로그램
The goal of this program is to provide expanded access (i.e., before marketing authorization) to tiratricol as treatment for patients with monocarboxylate transporter 8 deficiency (MCT8 deficiency, also known as Allan-Herndon-Dudley syndrome [AHDS]), who in their Treating Physician's opinion, could benefit from tiratricol and meet the eligibility criteria.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
This will be an open-label, single-arm, multi-center EAP, designed to provide treatment access in the US to tiratricol for eligible patients with MCT8 deficiency, also known as AHDS.
Patients will undergo clinical and safety assessments before tiratricol treatment initiation, during the titration phase and then at approximately 3-6 monthly intervals or more frequently if clinically indicated, following the initiation of tiratricol treatment and until treatment is completed or discontinued.
Adverse events (AEs) and serious adverse events (SAEs) will be recorded and reported as per FDA regulations.
연구 유형
연구 유형
확장 액세스 유형
확장 액세스 유형
- 개별 환자: 임상 시험에 참여할 수 없는 심각한 질병 또는 상태를 가진 단일 환자가 약물 또는 생물학적 제품에 대한 액세스를 허용합니다. FDA의 승인을 받지 않은 것입니다. 이 범주에는 응급 상황에서의 액세스도 포함됩니다.
- 중간 규모 인구: 한 명 이상의 환자(그러나 일반적으로 치료 IND/프로토콜을 통한 것보다 적은 수의 환자)가 FDA의 승인을 받지 않은 의약품 또는 생물학적 제제. 이러한 유형의 확장 액세스는 동일한 질병 또는 상태를 가진 여러 환자가 FDA의 승인을 받지 않은 특정 약물 또는 생물학적 제품에 대한 액세스를 모색할 때 사용됩니다.
- 치료 IND/프로토콜: 대규모의 광범위한 인구가 FDA의 승인을 받지 않은 의약품 또는 생물학적 제제에 접근할 수 있도록 허용합니다. 이러한 유형의 확장 액세스는 확장 액세스 사용과 동일한 용도로 마케팅을 위해 이미 제품이 개발되고 있는 경우에만 제공될 수 있습니다.
- 중간 규모 인구
- 치료 IND/프로토콜
연락처 및 위치
연구 장소
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Alabama
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Birmingham, Alabama, 미국, 35249
- University of Alabama at Birmingham Hospital
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California
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Madera, California, 미국, 93636-8762
- Valley Children's Hospital
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San Diego, California, 미국, 92123
- Rady Children's Hospital
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Florida
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Jacksonville, Florida, 미국, 32207
- Nemour's Children Hospital
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Georgia
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Atlanta, Georgia, 미국, 30329
- Children's Healthcare of Atlanta
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Illinois
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Chicago, Illinois, 미국, 60611
- Ann & Robert H. Lurie Children's Hospital of Chicago
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Louisiana
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New Orleans, Louisiana, 미국, 70118
- Louisiana State University Health Sciences Center and Children's Hospital
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Massachusetts
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Springfield, Massachusetts, 미국, 01199
- Baystate Medical Center
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Minnesota
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Saint Paul, Minnesota, 미국, 55101
- Gillette's Children's Specialty Healthcare
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New York
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New York, New York, 미국, 10029
- Icahn School of Medicine at Mount Sinai
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New York, New York, 미국, 10032
- Columbia University Irving Medical Center
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Oregon
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Portland, Oregon, 미국, 97239
- Oregon Health and Science University
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Pennsylvania
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Philadelphia, Pennsylvania, 미국, 19104
- Children's Hospital of Philadelphia
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Tennessee
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Memphis, Tennessee, 미국, 38105
- Le Bonheur Children's Hospital Foundation
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Texas
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Fort Worth, Texas, 미국, 76106
- Cook Children's Health Care System
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Washington
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Tacoma, Washington, 미국, 98403
- MultiCare Mary Bridge Children's Hospital
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Wisconsin
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Milwaukee, Wisconsin, 미국, 53326
- Children's Wisconsin
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
Each patient must meet all of the following criteria to be eligible:
- Diagnosis of MCT8 deficiency confirmed with a genetic test.
- Either tiratricol treatment naïve, or patients who may be on a stable dose of tiratricol having transferred from the Phase 3 MCT8-2021-3 (ReTRIACt) study (NCT05579327) or prior individual investigational new drug (IND).
- In the Treating Physician's medical opinion, the potential benefits of treatment with tiratricol outweigh the potential risks for the patient.
- Patient or legal representative provided signed and dated informed consent to be treated with tiratricol, through this EAP.
- Given the severity of the disease, sexual activity in these patients is deemed unlikely. However, where, at the discretion of the Treating Physician sexual activity is possible for the patient, patients must follow protocol-specified-contraception guidance.
- Patient is approved for enrolment by the sponsor RTT.
Exclusion Criteria:
Patients who meet any of the following criteria will be excluded from the EAP:
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Parents, legal representative or, if applicable, patients unwilling or unable to comply with the Treating Physician's treatment plan related to this EAP for any reason.
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Major illness or recent major surgery unrelated to MCT8 deficiency (in the Treating Physician's judgement), defined as:
- Conditions requiring repeated hospitalizations that are likely to confound ability to participate in the program.
- Major illness in the 3 months before the screening visit that is likely to confound the ability of the patient to participate fully within the program and/or confound the assessment of serum total T3 and/or safety.
- Major surgery within the 3 months before the screening visit, or planned to take place during the program, including but not limited to major abdominal/thoracic/neurosurgical procedures.
- Major/minor abdominal and/or maxillofacial surgery that may inhibit the administration and/or absorption of tiratricol.
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Patients with any contra-indication for treatment with tiratricol or any excipients in the program treatment.
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Patients using thyroid hormone analogues- such as levothyroxine -or thionamides, such as propylthiouracil. Prior use of these drugs is not an exclusion criterion, provided the use of the medication has subsided and the thyroid hormone levels have stabilized after the cessation of these medications. For patients currently using these medications the switch to tiratricol should be made following the above and under the guidance of an endocrinologist with knowledge of MCT8 deficiency, if needed, after consultation with pharmacologist.
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Known hypersensitivity to tiratricol including any ingredient in the pharmaceutical formulation.
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Although very unlikely, as this is a severe X-linked disease: Women who are nursing or pregnant (or women who are planning to become pregnant during treatment with tiratricol).
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Patients eligible for clinical trials with tiratricol.
공부 계획
연구는 어떻게 설계됩니까?
공동 작업자 및 조사자
협력자
협력자
간행물 및 유용한 링크
일반 간행물
- Groeneweg S, Peeters RP, Moran C, Stoupa A, Auriol F, Tonduti D, Dica A, Paone L, Rozenkova K, Malikova J, van der Walt A, de Coo IFM, McGowan A, Lyons G, Aarsen FK, Barca D, van Beynum IM, van der Knoop MM, Jansen J, Manshande M, Lunsing RJ, Nowak S, den Uil CA, Zillikens MC, Visser FE, Vrijmoeth P, de Wit MCY, Wolf NI, Zandstra A, Ambegaonkar G, Singh Y, de Rijke YB, Medici M, Bertini ES, Depoorter S, Lebl J, Cappa M, De Meirleir L, Krude H, Craiu D, Zibordi F, Oliver Petit I, Polak M, Chatterjee K, Visser TJ, Visser WE. Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial. Lancet Diabetes Endocrinol. 2019 Sep;7(9):695-706. doi: 10.1016/S2213-8587(19)30155-X. Epub 2019 Jul 31.
- van Geest FS, Groeneweg S, van den Akker ELT, Bacos I, Barca D, van den Berg SAA, Bertini E, Brunner D, Brunetti-Pierri N, Cappa M, Cappuccio G, Chatterjee K, Chesover AD, Christian P, Coutant R, Craiu D, Crock P, Dewey C, Dica A, Dimitri P, Dubey R, Enderli A, Fairchild J, Gallichan J, Garibaldi LR, George B, Hackenberg A, Heinrich B, Huynh T, Klosowska A, Lawson-Yuen A, Linder-Lucht M, Lyons G, Monti Lora F, Moran C, Muller KE, Paone L, Paul PG, Polak M, Porta F, Reinauer C, de Rijke YB, Seckold R, Menevse TS, Simm P, Simon A, Spada M, Stoupa A, Szeifert L, Tonduti D, van Toor H, Turan S, Vanderniet J, de Waart M, van der Wal R, van der Walt A, van Wermeskerken AM, Wierzba J, Zibordi F, Zung A, Peeters RP, Visser WE. Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study. J Clin Endocrinol Metab. 2022 Feb 17;107(3):e1136-e1147. doi: 10.1210/clinem/dgab750.
연구 기록 날짜
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
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마지막 업데이트 게시됨
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추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- Tiratricol-EAP-Pro MCT8-2022-4
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. .