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API CSV27행 · 1개 프로그램

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항목
AntibodyLimited DatastalePhase 2
Carmustine (Carmustine)
INSYS Therapeutics Inc·Human Immunodeficiency Virus 1 Pos…
122 trials
Overview
Program
Carmustine
Overview
Company
INSYS Therapeutics Inc
Overview
Modality
ANTIBODY
Overview
Target
Human Immunodeficiency Virus 1 Positive
Overview
Indication
Mantle Cell Lymphoma; Recurrent Diffuse Large B-Cell Lymphoma
Overview
Phase
PHASE_2
Overview
Status
DISCONTINUED
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
targeted nanodelivery system, denoted BCNU-FeSeH@EV LF , which integrates magnetic guidance, chemotactic homing, and receptor
MoA
Biomarker
biomarker for hepatocellular carcinoma,lung adenocarcinoma,and papillary renal cell carcinoma
PK/PD
Species
Rat
PK/PD
Animal (cat.)
Rat
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Rat
Toxicology
Animal (cat.)
Rat
Toxicology
Major finding
Toxicity and efficacy of four carmustine-substituted conditioning regimens followed by autologous stem cell transplantation in lymphoma: a real-world comparative study.. High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) remains a key consolidation strategy for patients with relapsed/refractory (R/R) lymphoma. The BEAM regimen (carmustine, etoposide, cytarabine, melphal…
Toxicology
CRS
Reported
Clinical
Safety signal
Toxicity and efficacy of four carmustine-substituted conditioning regimens followed by autologous stem cell transplantation in lymphoma: a real-world comparative study.. High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) remains a key consolidation strategy for patients with relapsed/refractory (R/R) lymphoma. The BEAM regimen (carmustine, etoposide, cytarabine, melphal…
Clinical
Selected reported efficacy
ORR 26%
Clinical
Reported ORR
26%
Clinical
Result source
ClinicalTrials.gov NCT00233987
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT00233987