U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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Showing 1631 - 1640 of 3321 results

mixture
Status:
Investigational
Source:
NCT04229979: Phase 3 Interventional Active, not recruiting Acute Myeloid Leukemia
(2021)
Source URL:

Class:
MIXTURE

mixture
Status:
Investigational
Source:
NCT03486990: Phase 2 Human clinical trial Completed N/A
Source URL:

Class:
MIXTURE

mixture
Status:
Investigational
Source:
NCT01900158: Phase 1 Interventional Completed Cholangiocarcinoma
(2013)
Source URL:

Class:
MIXTURE

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.
mixture
Status:
Designated
Source:
FDA ORPHAN DRUG:516316
Source URL:

Class:
MIXTURE

mixture
Status:
US Previously Marketed
First approved in 1985

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.
mixture
Status:
US Previously Marketed
Source:
Ananase by Rorer
(1962)
Source URL:
First approved in 1962
Source:
Ananase by Rorer
Source URL:

Class:
MIXTURE

mixture
Status:
US Previously Marketed
Source:
Tryptar by Armour
(1951)
Source URL:
First approved in 1951
Source:
Tryptar by Armour
Source URL:

Class:
MIXTURE

Showing 1631 - 1640 of 3321 results