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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

현재 선택: 1 · 임상 갱신 필요 1

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항목
CGTStandard DatabasestalePreclinical
methadone hydrochloride (methadone hydrochloride)
National Institute on Drug Abuse (…·Brain and Central Nervous System T…
61 trials·t½ 2.0 h
Overview
Program
methadone hydrochloride
Overview
Company
National Institute on Drug Abuse (NIDA)
Overview
Modality
CGT
Overview
Target
Brain and Central Nervous System Tumors
Overview
Indication
Brain and Central Nervous System Tumors; Chronic Myeloproliferative Disorders
Overview
Phase
PRECLINICAL
Overview
Status
DISCONTINUED
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Watch
Overview
Approval status
Investigational
MoA
Mechanism
target MORs such as novel low-efficacy MOR agonists or long-acting formulations, and (3) medications that target post-MOR signaling
MoA
Biomarker
biomarkers, long-term safety profiling, sex-specific responses, and real-world effectiveness studies
PK/PD
Half-life
2.0 h
PK/PD
Species
Dog, Ferret
PK/PD
Animal (cat.)
Dog
PK/PD
Experiment
Pharmacokinetic
Toxicology
Species
Dog, Ferret
Toxicology
Animal (cat.)
Dog
Toxicology
Major finding
Evaluation of thermal antinociceptive effects after intramuscular administration of methadone hydrochloride to orange-winged Amazon parrots (Amazona amazonica).. To evaluate the thermal antinociceptive effects of methadone after IM administration to orange-winged Amazon parrots (Amazona amazonica). 8 Amazon parrots received IM methadone hydrochloride (1, 3, and 6 mg/kg) and saline (0.9% NaCl) solu…
Clinical
Safety signal
Evaluation of thermal antinociceptive effects after intramuscular administration of methadone hydrochloride to orange-winged Amazon parrots (Amazona amazonica).. To evaluate the thermal antinociceptive effects of methadone after IM administration to orange-winged Amazon parrots (Amazona amazonica). 8 Amazon parrots received IM methadone hydrochloride (1, 3, and 6 mg/kg) and saline (0.9% NaCl) solu…
Clinical
Selected reported efficacy
ORR 13.7%
Clinical
Reported ORR
13.7%
Clinical
Result source
ClinicalTrials.gov NCT00386243
Clinical
Program phase
PRECLINICAL
Clinical
Trial ref
NCT00386243