Last reviewed · How we verify

Ketoprofen matrix/placebo CHADD Patch

ZARS Pharma Inc. · Phase 3 active Small molecule

Ketoprofen matrix/placebo CHADD Patch is a NSAID (nonsteroidal anti-inflammatory drug) Small molecule drug developed by ZARS Pharma Inc.. It is currently in Phase 3 development for Localized pain and inflammation (transdermal patch indication, likely musculoskeletal or arthritis-related pain). Also known as: ketoprofen matrix with no heat.

Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain.

Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain. Used for Localized pain and inflammation (transdermal patch indication, likely musculoskeletal or arthritis-related pain).

Likelihood of approval
59.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Immunology slight uplift +1.0pp
    Mature endpoint landscape (ACR, DAS28, PASI) makes immunology approvals slightly more predictable.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameKetoprofen matrix/placebo CHADD Patch
Also known asketoprofen matrix with no heat
SponsorZARS Pharma Inc.
Drug classNSAID (nonsteroidal anti-inflammatory drug)
TargetCOX-1, COX-2
ModalitySmall molecule
Therapeutic areaPain Management / Rheumatology
PhasePhase 3

Mechanism of action

Ketoprofen blocks COX-1 and COX-2 enzymes, which are responsible for producing prostaglandins that mediate inflammation, pain, and fever. The transdermal matrix patch formulation delivers ketoprofen through the skin to provide localized and/or systemic anti-inflammatory and analgesic effects. This delivery method aims to reduce systemic exposure compared to oral formulations while maintaining therapeutic efficacy.

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 Ketoprofen matrix/placebo CHADD Patch

What is Ketoprofen matrix/placebo CHADD Patch?

Ketoprofen matrix/placebo CHADD Patch is a NSAID (nonsteroidal anti-inflammatory drug) drug developed by ZARS Pharma Inc., indicated for Localized pain and inflammation (transdermal patch indication, likely musculoskeletal or arthritis-related pain).

How does Ketoprofen matrix/placebo CHADD Patch work?

Ketoprofen is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase (COX) enzymes to reduce prostaglandin synthesis, thereby decreasing inflammation and pain.

What is Ketoprofen matrix/placebo CHADD Patch used for?

Ketoprofen matrix/placebo CHADD Patch is indicated for Localized pain and inflammation (transdermal patch indication, likely musculoskeletal or arthritis-related pain).

Who makes Ketoprofen matrix/placebo CHADD Patch?

Ketoprofen matrix/placebo CHADD Patch is developed by ZARS Pharma Inc. (see full ZARS Pharma Inc. pipeline at /company/zars-pharma-inc).

Is Ketoprofen matrix/placebo CHADD Patch also known as anything else?

Ketoprofen matrix/placebo CHADD Patch is also known as ketoprofen matrix with no heat.

What drug class is Ketoprofen matrix/placebo CHADD Patch in?

Ketoprofen matrix/placebo CHADD Patch belongs to the NSAID (nonsteroidal anti-inflammatory drug) class. See all NSAID (nonsteroidal anti-inflammatory drug) drugs at /class/nsaid-nonsteroidal-anti-inflammatory-drug.

What development phase is Ketoprofen matrix/placebo CHADD Patch in?

Ketoprofen matrix/placebo CHADD Patch is in Phase 3.

What are the side effects of Ketoprofen matrix/placebo CHADD Patch?

Common side effects of Ketoprofen matrix/placebo CHADD Patch include Application site reactions (erythema, irritation), Gastrointestinal upset (if systemic absorption occurs), Headache, Dizziness.

What does Ketoprofen matrix/placebo CHADD Patch target?

Ketoprofen matrix/placebo CHADD Patch targets COX-1, COX-2 and is a NSAID (nonsteroidal anti-inflammatory drug).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing