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

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Showing 581 - 590 of 16236 results

Status:
Investigational
Source:
NCT02737904: Not Applicable Interventional Completed Multiple Sclerosis
(2016)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT01188967: Phase 2 Interventional Completed Nicotine Dependence
(2010)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
NCT01836029: Phase 2 Interventional Completed Carcinoma, Squamous Cell of Head and Neck
(2013)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Motolimod (VTX-2337) is a small molecule, selective Toll-like receptor (TLR) 8 agonist has been used in trials studying phase II for the treatment of peritoneal carcinoma, Ovarian Cancer, Fallopian Tube Cancer, B-cell lymphoma, squamous cell carcinoma of the head and neck among others. Motolimod is designed to mobilize a patient's immune system by directly activating myeloid dendritic cells, monocytes, and natural killer cells. This activation results in the production of a high level of mediators known to orchestrate the integration of both the innate and adaptive anti-tumor responses to a number of cancers.
Status:
Investigational
Source:
NCT01610388: Phase 1 Interventional Completed Infections, Bacterial
(2011)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

LANOPEPDEN is an inhibitor of peptide deformylase, a bacterial enzyme required for protein maturation. It was in development for the treatment of complicated bacterial skin infection and hospitalized community-acquired pneumonia.
Status:
Investigational
Source:
NCT04150250: Phase 2 Interventional Completed Cholera
(2019)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Conditions:

IOWH032 is a synthetic extracellular CFTR inhibitor, originally developed to treat diarrhea, that entered Phase II clinical trials in 2013 but did not progress further in clinical development. iOWH032 has low CFTR inhibition potency (IC50 > 5 uM) and hence rapid (seconds or less) dissociation from CFTR. iOWH032 inhibited secretion by nearly 70% as measured on a semi-quantitative fecal output scale.
Status:
Investigational
Source:
NCT00993421: Phase 2 Interventional Terminated Obesity
(2009)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)


LY377604 is a human β3-adrenergic receptor agonist and β1- and β2-adrenergic receptor antagonist with no sympathomimetic activity at the β1- and β2-adrenergic receptors. Combination of LY377604 and a norepinephrine-serotonin uptake inhibitor (sibutramine) was studied in the treatment of obesity. LY377604 would ameliorate side effect of sibutramine treatment (increase in blood pressure and heart rate due to activation of the sympathetic nervous system).
Status:
Investigational
Source:
NCT01345357: Phase 1 Interventional Completed Solid Tumors or Mantle Cell Lymphoma
(2011)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT01320787: Phase 1 Interventional Withdrawn Brain Cancer
(2014)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Fluoroacetic acid F-18 (18F-Fluoroacetate,18F-FAC) is an analog of acetate with a longer radioactive half-life (18F=110 min). Fluoroacetic acid F-18 was under investigation as a PET imaging agent. 18F-FAC was considered a promising alternative to 11C-ACE for positron tomographic imaging of prostate cancer, and possibly of other neoplasms with relatively low glucose use.
Status:
Investigational
Source:
NCT02415439: Phase 1 Interventional Completed Healthy
(2015)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
INN:iodofalan (131I) [INN]
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

The labeled 4-IODOPHENYLALANINE I-131 is used for proteomics research. It’s also can be used for the chemoselective modification of proteins.