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Indermil (ENBUCRILATE)

Phase 3 active Small molecule

Indermil (generic name: ENBUCRILATE) is a enbucrilate drug. It is currently in Phase 3 development.

Indermil works by forming a strong adhesive bond between the skin and the wound.

Indermil (Enbucrilate) is a small molecule enbucrilate drug used for its adhesive properties in wound closure and skin closure. It works by forming a strong bond between the skin and the wound, promoting healing and reducing the risk of infection. The commercial status of Indermil is not publicly available, and it is not clear if it is patented or available as a generic product. Indermil is used to treat skin wounds and closures, but its exact target and mechanism of action are not well-documented. As a result, key safety considerations and pharmacokinetic properties are not well-established.

Likelihood of approval
58.3% 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).
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 nameENBUCRILATE
Drug classenbucrilate
ModalitySmall molecule
Therapeutic areaDermatology
PhasePhase 3

Mechanism of action

Imagine a strong glue that helps hold your skin together while it heals. Indermil is like that glue, but it's a special medicine that helps your skin close up and heal faster. It's not something that gets absorbed into your body, but rather stays on the surface to do its job.

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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 Indermil

What is Indermil?

Indermil (ENBUCRILATE) is a enbucrilate drug.

How does Indermil work?

Indermil works by forming a strong adhesive bond between the skin and the wound.

What is the generic name of Indermil?

ENBUCRILATE is the generic (nonproprietary) name of Indermil.

What drug class is Indermil in?

Indermil belongs to the enbucrilate class. See all enbucrilate drugs at /class/enbucrilate.

What development phase is Indermil in?

Indermil is in Phase 3.

Related

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