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

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Showing 5981 - 5990 of 13362 results

Status:
Possibly Marketed Outside US
Source:
NCT02473406: Phase 4 Interventional Completed Pancreatitis, Acute Necrotizing
(2018)
Source URL:

Class:
PROTEIN

Thymalfasin, a synthetic version of thymosin-α-1, a polypeptide (protein fragment) was being developed by SciClone Pharmaceuticals for the treatment of liver disease. SciClone developed and launched Thymalfasin, under the trade name Zadaxin, for the treatment of hepatitis B and hepatitis C virus infections. The drug is also being developed for the treatment of non-small cell lung cancer (NSCLC), hepatocellular carcinoma, AIDS and malignant melanoma. Thymalfasin exerts a dual action against infections: immune modulating and direct-acting effect. Thymalfasin exerts its immune-modulating activity through the interaction with Toll-like receptors (TLR), a group of proteins involved in the regulation of innate immunity, and in particular with TLR9 and TLR2 on dendritic cells (DCs) and precursor T-cells. Thymalfasin is also able to prevent a pro-inflammatory cytokine storm and possibly autoimmune events. Regarding direct-acting effects, Thymalfasin has been shown to increase the expression of MHC Class I and II, which are important for the antigen presentation and recognition by the immune system of the virally infected cells. v has also been shown to directly inhibit the in vitro growth of virally infected and cancer cells. Thymalfasin is not approved by the FDA but it is widely used in China and some other countries.
Status:
Possibly Marketed Outside US
Source:
Japan:Teceleukin (Genetical Recombination)
Source URL:

Class:
PROTEIN

Status:
Possibly Marketed Outside US
Source:
NCT02234869: Phase 4 Interventional Withdrawn Relapsing Multiple Sclerosis
(2014)
Source URL:

Class:
PROTEIN

Calcitonin is a polypeptide hormone secreted by the parafollicular cells of the thyroid gland in mammals and studied in late 1970s postmenopausal osteoporosis treatment. The primary pharmacological effect of porcine calcitonin is its activity at specific osteoclast receptors, resulting in diminished osteoclast activity at extremely low concentrations and leading to the normalization of bone resorption and the formation and maintenance of functional bone. It also promotes the mineralization of bone, as acute studies in rats, rabbits and young pigs have shown, as well as exerting a regulatory effect on renal electrolyte excretion. The overall result is that bone mass is maintained or increased, with no adverse effect on cortical bone. In clinical trials porcine Calcitonin significantly increased the bone mineral density of the lumbar spine compared with placebo, but unfortunately did not influence the risk of new vertebral fractures.

Showing 5981 - 5990 of 13362 results