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세포·유전자 치료PreclinicalRecruiting

IMiD treatment

Sung-Soo Park

비교

IMiD treatment(Sung-Soo Park)은 FRα 표적 세포·유전자 치료로, Multiple Myeloma, Relapsed; Multiple Myeloma (MM) 영역에서 개발·상용화 중입니다. 작용기전: that likely involves a tightly coordinated regulation of CRBN with endothelial cell targets and highlight the need to further elucidate the mechanism(s), which could include cerebl. 전임상 단계입니다. 대표 임상 효능: ORR 26.2% (ClinicalTrials.gov NCT02336815). 차별점: first-in-class IRAK4 heterobifunctional degrader that utilizes cereblon (CRBN) for E3 ligase recruitment and was rationally designed t.

출처: ClinicalTrials.gov · PubMed · openFDA최근 동기화됨

개요

임상 2026년 7월 13일 (1일 전)PK/독성 2026년 7월 13일 (1일 전)

FRα

Multiple Myeloma, Relapsed; Multiple Myeloma (MM)

Recruiting

Technology

bispecific antibodies, and chimeric antigen receptor T cells)

first-in-class IRAK4 heterobifunctional degrader that utilizes cereblon (CRBN) for E3 ligase recruitment and was rationally designed t

Mechanism of Action

that likely involves a tightly coordinated regulation of CRBN with endothelial cell targets and highlight the need to further elucidate the mechanism(s), which could include cereblon-independent pathways, through which

immune-mediated inflammatory diseases

apoptosis, which was associated with decreased IRF4, c-Myc, and phosphorylated STAT3 levels as well as enhanced SOCS3 expression

biomarkers of Mtb burden or Mtb clearance in patients with different TB status and different risk to develop

resistance to traditional IMiDs has become more prevalent, creating an urgent need for next-generation cereblon E3 ligase modulators

임상시험 & 결과

차트 로드 중…

임상 한눈에 보기

  • 39건의 ClinicalTrials.gov 임상 기록
  • Phase·Status 요약은 enrollment 상위 표본 기준입니다
  • 임상시험 탭에서 enrollment 상위 목록을 불러올 수 있습니다
  • Phase: Phase 2 · Phase 3 · Phase 1
  • Status: Unknown status · Completed · Not yet recruiting
  • 주요 endpoint: Occurrence of incident second IMID · All the individual subtypes of second IMIDs included in the primary outcome definition · IGRA positivity · IGRA conversion · Incidence of hyperpigmentation in Black participants exposed to IMiDs to non-IMiDs for MM
  • 등록된 결과: ORR 26.2%
  • 핵심: This is a Phase 2b, single-arm, open-label, multicenter study of selinexor 80 mg plus dexamethasone 20 mg (Sd) dosed twi…

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

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

참고문헌

자주 묻는 질문

IMiD treatment은 어떤 치료제인가요?
IMiD treatment(Sung-Soo Park)은 FRα 표적 세포·유전자 치료로, Multiple Myeloma, Relapsed; Multiple Myeloma (MM) 영역에서 개발·상용화 중입니다. 데이터는 바이오모아 (BioMoa)에서 ClinicalTrials.gov·openFDA·PubMed 기반으로 정리합니다.
IMiD treatment의 임상 단계는?
IMiD treatment의 현재 단계는 Preclinical입니다.
비슷한 프로그램과 어떻게 비교하나요?
바이오모아 (BioMoa) 비교 페이지에서 PK/PD, 독성, 임상 효능 지표를 나란히 볼 수 있습니다. 동일 타깃·모달리티 프리셋을 함께 참고하세요.