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

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Showing 21 - 30 of 81 results

Status:
Investigational
Source:
NCT01854294: Phase 2 Interventional Completed Amyotrophic Lateral Sclerosis
(2013)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

GM-602 (GM6) is a six-amino-acid active analog peptide of Motoneuronotrophic factor (MNTF). This compound is a small peptide that can cross the blood-brain barrier and has been shown to induce an embryonic-like neuroprotective microenvironment that helps detect and self-correct CNS- and neurodegenerative-related pathophysiology. Phase II clinical trials with GM-602, GM-604 and GM-608 have been completed to examine its potential in respectively stroke, Amyotrophic Lateral Sclerosis (ALS), and Parkinson’s disease.
Status:
Investigational
Source:
NCT04297683: Phase 2/Phase 3 Interventional Active, not recruiting Amyotrophic Lateral Sclerosis
(2020)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



Pridopidine is an experimental drug candidate belonging to a class of agents known as dopidines, which act as dopaminergic stabilizers in the central nervous system. As a dopamine stabilizer, pridopidine is thought to reduce the effects of dopamine when there’s too much and increase its effects when there’s too little. Pridopidine, therefore, plays two opposing roles in the brain, which stabilize dopamine levels. In this way, pridopidine is thought to help the brain reestablish a normal balance of neurotransmitters, and thus regain control over motion. Pridopidine intended to treat Huntington’s disease movement symptoms. Pridopidine was well tolerated and had an adverse event profile similar to a placebo.
Status:
Designated
Source:
FDA ORPHAN DRUG:872722
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Designated
Source:
FDA ORPHAN DRUG:884922
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



ZLN005 was developed as a novel small molecule, led to changes in peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) mRNA levels, glucose uptake, and fatty acid oxidation in L6 myotubes. ZLN005 exerted promising therapeutic effects for treating type 2 diabetes. ZLN005 increases fat oxidation and improves the glucose tolerance, pyruvate tolerance, and insulin sensitivity of diabetic db/db mice. In addition, was confirmed potential of PGC-1α as a drug target for the treatment of type 2 diabetes mellitus (T2DM) and metabolic syndromes.
Status:
Designated
Source:
FDA ORPHAN DRUG:844521
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Designated
Source:
FDA ORPHAN DRUG:802820
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Designated
Source:
FDA ORPHAN DRUG:704119
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Designated
Source:
EU-Orphan Drug:EU/3/12/954
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
US Previously Marketed
Source:
21 CFR 310.545(a)(20) weight control tryptophan
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)



Tryptophan is alpha-aminoacid that is used in the biosynthesis of proteins. It is essential aminoacid in humans, meaning the body cannot synthesize and it must be obtained from the diet. Tryptophan is a precursor of serotonin, and as such is sold over the counter in many countries as a dietary supplement for use as an antidepressant, anxiolytic and sleep aid, however application of tryptophan in these indications is not approved by FDA.