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Phase 1Active

AdV-tk

Candel TherapeuticsInc.

비교

AdV-tk(Candel Therapeutics, Inc.)은 Glioma, Malignant 표적 치료제로, Malignant Glioma; Recurrent Ependymoma 영역에서 개발·상용화 중입니다. Phase 1 안전성·PK 탐색 단계입니다. PFS: 0. 차별점: Novel permissive murine immunocompetent orthotopic colon carcinoma model for comparison of the antitumoral and safety profile.

출처: ClinicalTrials.gov · PubMed · openFDA최근 동기화됨

개요

임상 2026년 7월 18일 (8일 전)PK/독성 2026년 7월 18일 (8일 전)

Glioma, Malignant

Malignant Glioma; Recurrent Ependymoma

Active

Technology

gene therapy

adenoviral vector into four sites in the prostate was practical as an outpatient procedure

Novel permissive murine immunocompetent orthotopic colon carcinoma model for comparison of the antitumoral and safety profile

Mechanism of Action

cytokine release syndrome (CRS)

apoptosis and inhibiting angiogenesis, and is a promising treatment strategy for hepatic carcinoma

biomarkers were evaluated in tumor and blood before and after GMCI

escape

임상시험 & 결과

차트 로드 중…

임상 한눈에 보기

  • 32건의 ClinicalTrials.gov 임상 기록
  • Phase·Status 요약은 enrollment 상위 표본 기준입니다
  • 임상시험 탭에서 enrollment 상위 목록을 불러올 수 있습니다
  • Phase: Phase 1 · Phase 3 · Phase 2 · Phase 1, Phase 2
  • Status: Completed · Available · Active, not recruiting
  • 주요 endpoint: Disease free survival defined as the time from randomization until the date of the first failure event will be compared for the ProstAtak® arm versus the placebo control arm. The analyses will be based on the intent to treat population. · Prostate cancer specific survival and overall survival will be compared for the ProstAtak® arm versus the placebo control arm. · PSA nadir will be compared for the ProstAtak® arm versus the placebo control arm. · Patient reported Health Related Quality of Life outcomes will be collected using the Expanded Prostate Cancer Index Composite (EPIC-26) questionnaire. The change in QOL over time will be compared for the ProstAtak® arm versus the placebo control arm. · The safety profile will be characterized by collection of adverse event information and laboratory values during the treatment phase (until the completion of radiation). Data on late effects will be collected after radiation completion.
  • 등록된 결과: ORR 11%
  • PFS: 0
  • 핵심: This is a Phase II trial to determine the efficacy and safety of in situ gene therapy and stereotactic body radiation th…

임상시험이 많습니다. 임상시험 탭에서 Phase/Status 필터·검색을 사용하세요.

수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.

참고문헌

자주 묻는 질문

AdV-tk은 어떤 치료제인가요?
AdV-tk(Candel Therapeutics, Inc.)은 Glioma, Malignant 표적 항체로, Malignant Glioma; Recurrent Ependymoma 영역에서 개발·상용화 중입니다. 데이터는 바이오정보모아 (BioJungboMoa)에서 ClinicalTrials.gov·openFDA·PubMed 기반으로 정리합니다.
AdV-tk의 임상 단계는?
AdV-tk의 현재 단계는 Phase 1입니다.
비슷한 프로그램과 어떻게 비교하나요?
바이오정보모아 (BioJungboMoa) 비교 페이지에서 PK/PD, 독성, 임상 효능 지표를 나란히 볼 수 있습니다. 동일 타깃·모달리티 프리셋을 함께 참고하세요.