Last reviewed · How we verify

Diclofenac diethylamine 2.32% gel

GlaxoSmithKline · Phase 3 active Small molecule

Diclofenac diethylamine 2.32% gel is a Nonsteroidal anti-inflammatory drug (NSAID) Small molecule drug developed by GlaxoSmithKline. It is currently in Phase 3 development for Topical treatment of localized pain and inflammation associated with musculoskeletal conditions (e.g., sprains, strains, osteoarthritis).

Diclofenac diethylamine is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain at the site of application.

Diclofenac diethylamine is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain at the site of application. Used for Topical treatment of localized pain and inflammation associated with musculoskeletal conditions (e.g., sprains, strains, osteoarthritis).

At a glance

Generic nameDiclofenac diethylamine 2.32% gel
SponsorGlaxoSmithKline
Drug classNonsteroidal anti-inflammatory drug (NSAID)
TargetCyclooxygenase-1 (COX-1) and Cyclooxygenase-2 (COX-2)
ModalitySmall molecule
Therapeutic areaPain Management / Rheumatology
PhasePhase 3

Mechanism of action

Diclofenac works by blocking COX-1 and COX-2 enzymes, which are responsible for producing prostaglandins that mediate inflammation, pain, and fever. The diethylamine salt formulation enhances skin penetration when applied topically as a gel, allowing the active drug to reach affected tissues. This localized delivery minimizes systemic exposure compared to oral NSAIDs.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Diclofenac diethylamine 2.32% gel

What is Diclofenac diethylamine 2.32% gel?

Diclofenac diethylamine 2.32% gel is a Nonsteroidal anti-inflammatory drug (NSAID) drug developed by GlaxoSmithKline, indicated for Topical treatment of localized pain and inflammation associated with musculoskeletal conditions (e.g., sprains, strains, osteoarthritis).

How does Diclofenac diethylamine 2.32% gel work?

Diclofenac diethylamine is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain at the site of application.

What is Diclofenac diethylamine 2.32% gel used for?

Diclofenac diethylamine 2.32% gel is indicated for Topical treatment of localized pain and inflammation associated with musculoskeletal conditions (e.g., sprains, strains, osteoarthritis).

Who makes Diclofenac diethylamine 2.32% gel?

Diclofenac diethylamine 2.32% gel is developed by GlaxoSmithKline (see full GlaxoSmithKline pipeline at /company/gsk).

What drug class is Diclofenac diethylamine 2.32% gel in?

Diclofenac diethylamine 2.32% gel belongs to the Nonsteroidal anti-inflammatory drug (NSAID) class. See all Nonsteroidal anti-inflammatory drug (NSAID) drugs at /class/nonsteroidal-anti-inflammatory-drug-nsaid.

What development phase is Diclofenac diethylamine 2.32% gel in?

Diclofenac diethylamine 2.32% gel is in Phase 3.

What are the side effects of Diclofenac diethylamine 2.32% gel?

Common side effects of Diclofenac diethylamine 2.32% gel include Local skin irritation or erythema, Contact dermatitis, Photosensitivity.

What does Diclofenac diethylamine 2.32% gel target?

Diclofenac diethylamine 2.32% gel targets Cyclooxygenase-1 (COX-1) and Cyclooxygenase-2 (COX-2) and is a Nonsteroidal anti-inflammatory drug (NSAID).

Related