Last reviewed · How we verify

Advantan (METHYLPREDNISOLONE ACEPONATE)

Phase 2 active Small molecule

Advantan (generic name: METHYLPREDNISOLONE ACEPONATE) is a Corticosteroid drug. It is currently in Phase 2 development.

Advantan works by binding to glucocorticoid receptors in the body, which then suppresses the production of inflammatory chemicals.

Advantan (METHYLPREDNISOLONE ACEPONATE) is a corticosteroid medication developed by Schering-Plough, currently owned by Merck & Co. It is a small molecule that works by suppressing the immune system to reduce inflammation and swelling. Advantan is used to treat various skin conditions, including eczema and atopic dermatitis. The commercial status of Advantan is patented, and its safety considerations include potential side effects such as skin thinning and increased risk of infections. As a corticosteroid, Advantan should be used under medical supervision to minimize risks.

Likelihood of approval
16.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% 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 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +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 nameMETHYLPREDNISOLONE ACEPONATE
Drug classCorticosteroid
ModalitySmall molecule
Therapeutic areaImmunology
PhasePhase 2

Mechanism of action

Imagine your immune system is like a fire alarm that goes off when it senses something wrong. Advantan helps turn down the volume on the fire alarm, reducing the inflammation and swelling that can cause discomfort and pain. This allows the skin to heal and recover more quickly.

Approved indications

No approved indications tracked.

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 Advantan

What is Advantan?

Advantan (METHYLPREDNISOLONE ACEPONATE) is a Corticosteroid drug.

How does Advantan work?

Advantan works by binding to glucocorticoid receptors in the body, which then suppresses the production of inflammatory chemicals.

What is the generic name of Advantan?

METHYLPREDNISOLONE ACEPONATE is the generic (nonproprietary) name of Advantan.

What drug class is Advantan in?

Advantan belongs to the Corticosteroid class. See all Corticosteroid drugs at /class/corticosteroid.

What development phase is Advantan in?

Advantan is in Phase 2.

What are the side effects of Advantan?

Common side effects of Advantan include Steroid withdrawal syndrome, Euphoric mood, Pelvic venous thrombosis, Coagulation test abnormal, Stupor, Erythrodermic psoriasis.

Related

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