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Kenalog and Sensorcaine

Horizon Health Network · Phase 3 active Small molecule Under review

Kenalog and Sensorcaine is a Corticosteroid + Local anesthetic combination Small molecule drug developed by Horizon Health Network. It is currently in Phase 3 development for Intra-articular injection for inflammatory joint conditions (e.g., rheumatoid arthritis, osteoarthritis), Soft-tissue injection for localized inflammation and pain relief. Also known as: Kenalog, Triamcinolone, Sensorcaine, Marcaine.

This is a combination of a corticosteroid (triamcinolone acetonide) and a local anesthetic (bupivacaine) for intra-articular or soft-tissue injection to reduce inflammation and provide pain relief.

Kenalog and Sensorcaine are used in a peripheral nerve block, specifically in a treatment for medication overuse headaches, as part of a clinical trial comparing its effects to Topamax.

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 nameKenalog and Sensorcaine
Also known asKenalog, Triamcinolone, Sensorcaine, Marcaine, Bupivacaine hydrochloride
SponsorHorizon Health Network
Drug classCorticosteroid + Local anesthetic combination
TargetGlucocorticoid receptor (triamcinolone); Voltage-gated sodium channels (bupivacaine)
ModalitySmall molecule
Therapeutic areaRheumatology / Pain Management / Orthopedics
PhasePhase 3

Mechanism of action

Kenalog (triamcinolone acetonide) is a synthetic corticosteroid that suppresses local inflammatory responses by inhibiting phospholipase A2 and reducing prostaglandin and leukotriene production. Sensorcaine (bupivacaine) is a long-acting amide local anesthetic that blocks sodium channels in nerve membranes, preventing depolarization and pain signal transmission. Together, they provide both anti-inflammatory and analgesic effects at the injection site.

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 Kenalog and Sensorcaine

What is Kenalog and Sensorcaine?

Kenalog and Sensorcaine is a Corticosteroid + Local anesthetic combination drug developed by Horizon Health Network, indicated for Intra-articular injection for inflammatory joint conditions (e.g., rheumatoid arthritis, osteoarthritis), Soft-tissue injection for localized inflammation and pain relief.

How does Kenalog and Sensorcaine work?

This is a combination of a corticosteroid (triamcinolone acetonide) and a local anesthetic (bupivacaine) for intra-articular or soft-tissue injection to reduce inflammation and provide pain relief.

What is Kenalog and Sensorcaine used for?

Kenalog and Sensorcaine is indicated for Intra-articular injection for inflammatory joint conditions (e.g., rheumatoid arthritis, osteoarthritis), Soft-tissue injection for localized inflammation and pain relief.

Who makes Kenalog and Sensorcaine?

Kenalog and Sensorcaine is developed by Horizon Health Network (see full Horizon Health Network pipeline at /company/horizon-health-network).

Is Kenalog and Sensorcaine also known as anything else?

Kenalog and Sensorcaine is also known as Kenalog, Triamcinolone, Sensorcaine, Marcaine, Bupivacaine hydrochloride.

What drug class is Kenalog and Sensorcaine in?

Kenalog and Sensorcaine belongs to the Corticosteroid + Local anesthetic combination class. See all Corticosteroid + Local anesthetic combination drugs at /class/corticosteroid-local-anesthetic-combination.

What development phase is Kenalog and Sensorcaine in?

Kenalog and Sensorcaine is in Phase 3.

What are the side effects of Kenalog and Sensorcaine?

Common side effects of Kenalog and Sensorcaine include Local injection site reactions (pain, swelling, erythema), Transient increase in joint pain (post-injection flare), Infection at injection site, Systemic corticosteroid effects (with repeated injections).

What does Kenalog and Sensorcaine target?

Kenalog and Sensorcaine targets Glucocorticoid receptor (triamcinolone); Voltage-gated sodium channels (bupivacaine) and is a Corticosteroid + Local anesthetic combination.

Related

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