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Cenegermin

Recombinant Human Nerve Growth Factor — SENSORY ORGANS

Also known as: oxervate

EMA approvedOrphan designationATC S01XA24

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Cenegermin is a drug in the Recombinant Human Nerve Growth Factor class catalogued in DrugCentral. It was first approved by the EMA in 2017. DrugCentral lists 2 molecular targets, including NTRK1 and NGFR. Recorded indications include Neurotrophic keratitis.

  • Drug class: Recombinant Human Nerve Growth Factor.
  • Molecular targets: NTRK1 and NGFR (2 listed in DrugCentral).
  • Indications: Neurotrophic keratitis.
  • ATC code: S01XA24 (Other ophthalmologicals).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Neurotrophic keratitis

Mechanism & targets

Established pharmacologic classRecombinant Human Nerve Growth Factor

Molecular targets (2)

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2017-07-06EMA—Dompe farmaceutici s.p.a.Yes

ATC classification

ATC codeTherapeutic hierarchy
S01XA24SENSORY ORGANS › OPHTHALMOLOGICALS › OTHER OPHTHALMOLOGICALS › Other ophthalmologicals

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Eye pain2491.6
Eye irritation694.9
Ocular hyperaemia528.1
Photophobia369.8
Ocular discomfort357.0
Eyelid pain329.0
Periorbital pain253.1
Eye swelling232.1
Corneal deposits229.4
Vision blurred225.1
Therapy interrupted207.7
Product dose omission issue198.9

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID—

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Cenegermin used for?

DrugCentral lists the following indications for Cenegermin: Neurotrophic keratitis.

How does Cenegermin work?

Its molecular targets in DrugCentral include NTRK1 (agonist) and NGFR (agonist).

When was Cenegermin first approved?

Cenegermin was first approved by the EMA in 2017.

What drug class does Cenegermin belong to?

Cenegermin is in the Recombinant Human Nerve Growth Factor class.

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Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2017-07-06
AgencyEMA
Targets2
Indications1
Formula—
DrugCentral ID5235
Interactive profile