← 홈

프로그램 비교

타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-5 · 마지막 9월 2일

현재 선택: 1 · 임상 갱신 필요 1

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV25행 · 1개 프로그램

표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.

항목
CGTStandard DatabasestalePhase 1
KYV-101 (KYV-101, Biological, KYV-101 (Biological) - 0.33 ×10^8 cells)
Kyverna Therapeutics·Progressive Multiple Sclerosis
133 trials
Overview
Program
KYV-101 (Biological) - 0.33 ×10^8 cells
Overview
Company
Kyverna Therapeutics
Overview
Modality
CGT
Overview
Target
Progressive Multiple Sclerosis
Overview
Indication
Progressive Multiple Sclerosis
Overview
Phase
PHASE_1
Overview
Status
RECRUITING
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Watch
Overview
Approval status
Investigational
MoA
Mechanism
, clinical efficacy, and safety of mosunetuzumab, an agent representative of immunotherapeutic advancement in lymphoma
MoA
Biomarker
EGFR2 gene expression
PK/PD
Species
Rat
PK/PD
Animal (cat.)
Rat, In vitro
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Rat
Toxicology
Animal (cat.)
Rat, In vitro
Toxicology
Major finding
Prevalence and clinical relevance of anti-drug antibodies in psoriatic arthritis: a systematic review.. To determine the prevalence of anti-drug antibodies (ADAs) in patients with psoriatic arthritis (PsA) treated with biological disease-modifying antirheumatic drugs (bDMARDs) and to evaluate associations with serum drug levels, clinical efficacy and safety. A Preferred Reporting Items for Systema…
Clinical
Safety signal
Prevalence and clinical relevance of anti-drug antibodies in psoriatic arthritis: a systematic review.. To determine the prevalence of anti-drug antibodies (ADAs) in patients with psoriatic arthritis (PsA) treated with biological disease-modifying antirheumatic drugs (bDMARDs) and to evaluate associations with serum drug levels, clinical efficacy and safety. A Preferred Reporting Items for Systema…
Clinical
Selected reported efficacy
92.9%
Clinical
Result source
ClinicalTrials.gov NCT05966090
Clinical
Program phase
PHASE_1
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT05966090