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Search results for "ORPHAN DRUG" in comments (approximate match)
Status:
Investigational
Source:
NCT04229979: Phase 3 Interventional Active, not recruiting Acute Myeloid Leukemia
(2021)
Source URL:
Class:
MIXTURE
Status:
Investigational
Source:
NCT03486990: Phase 2 Human clinical trial Completed N/A
Source URL:
Class:
MIXTURE
Status:
Investigational
Source:
NCT01900158: Phase 1 Interventional Completed Cholangiocarcinoma
(2013)
Source URL:
Class:
MIXTURE
Status:
Designated
Source:
FDA ORPHAN DRUG:485715
Source URL:
Class:
MIXTURE
3-Butylidenephthalide is a gamma-lactone isolated from Angelica sinensis, which is used to treat anemia and gynecological dysfunction in traditional Chinese medicine. 3-Butylidenephthalide is a natural liposoluble compound with a low molecular weight that possesses multiple pharmacological activities, such as reducing injury and fibrosis in the liver and neuroprotective activity. 3-Butylidenephthalide exerts cytotoxic or inhibitory effects on various cancers, including brain, lung, colon, prostate, and liver cancers.
Status:
Designated
Source:
FDA ORPHAN DRUG:516316
Source URL:
Class:
MIXTURE
Status:
Designated
Source:
FDA ORPHAN DRUG:623717
Source URL:
Class:
MIXTURE
Status:
US Previously Marketed
Source:
MOCTANIN by ETHITEK
(1985)
Source URL:
First approved in 1985
Source:
MOCTANIN by ETHITEK
Source URL:
Class:
MIXTURE
Conditions:
Glyceryl 1-caprylate (Monooctanoin, Capmul 8210), a semisynthetic esterified glycerol, a cholesterol solvent, that has been used for the dissolution of retained cholesterol gallstones following cholecystectomy. Bile duct infusion of monooctanoin is associated with little toxicity, although potentially serious problems can result from absorption of the drug or tissue infiltration. Gastrointestinal side effects such as anorexia, nausea, vomiting, diarrhea, and abdominal pain have been reported most commonly. Complete gallstone dissolution has occurred in approximately 50-75 percent of patients receiving monooctanoin. Although mechanical stone removal is still considered to be the treatment of choice for retained gallstones, monooctanoin use appeared promising for stone dissolution in patients in whom mechanical removal has been unsuccessful or is impossible. Monoctanoin was approved by the U.S. Food and Drug Administration (FDA) on Oct 29, 1985. It was developed and marketed as Moctanin® by ETHITEK in US.
Status:
First approved in 1962
Class:
MIXTURE
Status:
First approved in 1951
Class:
MIXTURE
Status:
US Previously Marketed
Source:
Amyl Nitrite U.S.P.
(1880)
Source URL:
First marketed in 1880
Source:
Amyl Nitrite U.S.P.
Source URL:
Class:
MIXTURE