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Topical diclofenac sodium gel

Guang'anmen Hospital of China Academy of Chinese Medical Sciences · FDA-approved active Small molecule

Diclofenac sodium inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain at the site of topical application.

Diclofenac sodium inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain at the site of topical application. Used for Localized musculoskeletal pain and inflammation, Osteoarthritis pain (topical), Rheumatoid arthritis pain (topical).

At a glance

Generic nameTopical diclofenac sodium gel
SponsorGuang'anmen Hospital of China Academy of Chinese Medical Sciences
Drug classNonsteroidal anti-inflammatory drug (NSAID)
TargetCOX-1 and COX-2 enzymes
ModalitySmall molecule
Therapeutic areaPain Management / Rheumatology
PhaseFDA-approved

Mechanism of action

As a nonsteroidal anti-inflammatory drug (NSAID), diclofenac blocks COX-1 and COX-2 enzymes, which are responsible for producing prostaglandins that mediate inflammation, pain, and fever. When applied topically as a gel, it penetrates local tissues to provide anti-inflammatory and analgesic effects with minimal systemic absorption, making it suitable for localized musculoskeletal and joint pain.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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