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

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Showing 51 - 60 of 2551 results

Status:
Investigational
Source:
USAN:SUNIRINE [USAN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
INN:famlasertib [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
INN:fenharmane [INN]
Source URL:

Class (Stereo):
CHEMICAL (UNKNOWN)

FENHARMANE, a reserpine-like substance, is a neuroleptic developed and clinically tested in the Czech Republic.
Status:
Investigational
Source:
INN:darglitazone
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)



Darglitazone is a member of the thiazolidinedione class of drugs and an agonist of peroxisome proliferator-activated receptor-γ (PPAR-γ), an orphan member of the nuclear receptor superfamily of transcription factors. It has a variety of insulin-sensitizing effects, such as improving glycemic and lipidemic control, and is used in the treatment of metabolic disorders such as type II diabetes. Darglitazone sodium had been in phase I clinical trials by Pfizer for the treatment of type 2 diabetes. However, this study has been discontinued.
Status:
Investigational
Source:
NCT03180528: Phase 2 Interventional Completed Skin Basal Cell Carcinoma
(2018)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

METHYLPARABEN SUBEROHYDROXAMIC ACID PHENYL ESTER (more known as Remetinostat), a histone deacetylase (HDAC) inhibitor, was developed for the treatment of cutaneous T cell lymphoma (CTCL). This drug is participating in phase II clinical trial to evaluate the efficacy, safety, and tolerability to skin lesions in patients with early-stage cutaneous T-cell lymphoma. In May 2019 was announced the positive results from phase II trial of remetinostat in basal cell carcinoma (BCC) patients. Initial results suggest that remetinostat gel offers a potentially effective and well-tolerated, non-surgical intervention for the treatment of localized BCCs. The unique design of remetinostat enables topical application, making it active only in the skin. As soon as it reaches the blood stream, it is degraded, avoiding the side effects associated with other HDAC inhibitors. Besides, remetinostat was studied as the treatment of plaque psoriasis; however, this study was discontinued.
Status:
Investigational
Source:
INN:sulfonterol [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Sulfonterol is a benzenemethanol derivative patented by Smith Kline and French Laboratories as a bronchodilator. Sulfonterol acts as a β-adrenergic partial agonist.
Status:
Investigational
Source:
INN:indocate [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Indocate is indole derivative and monoamine oxidase inhibitor with peripheral antiserotonin properties.
Status:
Investigational
Source:
INN:fosquidone
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Fosquidone (also known as GR63178A), a pentacyclic pyrroloquinone that was developed as an anticancer agent. Fosquidone participated in phase II clinical trial for the treatment of patients with colorectal, renal and non-small cell lung cancer. However, the drug didn’t show significant antitumor activity. The further development of this drug was discontinued.
Status:
Investigational
Source:
INN:propanocaine
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Propanocaine is a benzyl alcohol derivative with local anesthetics activity
Status:
Investigational
Source:
INN:fepitrizol [INN]
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

FEPITRIZOL is a hypnotic agent.