Drug intelligence / Profile preview

Nutrilarm

Development stage
Unknown
Lead developer
Théa Pharmaceuticals
Modality
Small Molecules
Administration
Oral
01

Overview

Nutrilarm (T1675) is an oral dietary supplement developed by Laboratoires Thea specifically for the management of dry eye syndrome. The formulation consists of a combination of omega-3 polyunsaturated fatty acids, including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), and omega-6 polyunsaturated fatty acids, including gamma-linolenic acid (GLA) and linoleic acid (LA). These essential fatty acids act as precursors to anti-inflammatory mediators, helping to modulate the inflammatory processes on the ocular surface that characterize dry eye disease. Clinical evaluation in a Phase 2 trial demonstrated that Nutrilarm, when used as a 6-month dietary supplement, provides additional therapeutic benefits such as improved tear break-up time (TBUT) and reduced ocular fatigue in patients already receiving topical tear substitutes.

Brand names
Nutrilarm
Other names
T1675 dietary formulationT-1675 dietary formulationT 1675 dietary formulationT1675 food supplementT-1675 food supplementT 1675 food supplement
02

Targets

ALOX12 (Arachidonate 12-lipoxygenase, 12S type)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)

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