idoxuridine

Trade name: herplex

Small moleculeapproved

Approved

Jun 11, 1963

Idoxuridine is an antiviral agent use in keratitis caused by herpes simplex virus. As a prescription drug it comes as a 0.1% ophthalmic solution/drops (Herplex and Dendrid). The first studies of the compound for treatment of human herpes simplex started in early 1960s. Being a structural analog of thymidine idoxuridine inhibits viral DNA replication by substituting thymidine. The effect of idoxuridine results in the inability of the virus to reproduce and/or infect tissues. Idoxuridine also blocks viral thymidine kinase as its substrate analog. — NCATS

Clinical trial activity

2 trials · 3 clinical orgs · 3 marketing orgs

Phase 1
1
Phase 2
1
Phase 3
0
Phase 4
0

Earliest trial started Mar 1, 1997 (NCT00109785)

Timeline

1960s

  1. Jun 11, 1963

    Allergan — Earliest FDA Approval

  2. Jun 11, 1963

    Allergan — NDA Secondary Org

  3. Jun 11, 1963

    Allergan — NDA Organization

  4. Jun 28, 1963

    Alcon — NDA Secondary Org

  5. Apr 6, 1964

    GlaxoSmithKline — Marketing Organization

  6. Apr 6, 1964

    GlaxoSmithKline — NDA Secondary Org

1990s

  1. Jan 1, 1997

    Earliest Phase 1 Sponsor(trial)

  2. Jan 1, 1998

    Earliest Phase 2 Sponsor(trial)

Indications

Mechanism of action

  • DNAINHIBITOR

    DNA inhibitor

    Incorporation into DNA

Approval history

  • approvedPriority reviewJun 11, 1963

Chemistry & pharmacology

Loading structure…

SMILES

OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(I)C(=O)NC2=O
Mol. weight
354.0985 g/mol
Lipinski Ro5
Pass
Rule of 3
No
Chirality
Single Stereoisomer
Inorganic
No
Polymer
No
Delivery
Topical
Availability
Discontinued

Oral

No

Parenteral

No

Topical

Yes

Sources

Also known as

  • 1-(2-deoxy-beta-d-ribofuranosyl)-5-iodouracil
  • 1-(2-deoxy-beta-d-ribofuranosyl)-5-iodouracil
  • 1-beta-d-2'-deoxyribofuranosyl-5-iodouracil
  • 1-beta-d-2'-deoxyribofuranosyl-5-iodouracil
  • 1beta-d-2'-deoxyribofuranosyl-5-iodouracil
  • 1beta-d-2'-deoxyribofuranosyl-5-iodouracil
  • 2'-deoxy-5-iodouridine
  • 2'-deoxy-5-iodouridine
  • 5-fluorodeoxyuridine
  • 5-fluorodeoxyuridine
  • 5-fluorodeoxyuridine
  • (+)-5-iodo-2'-deoxyuridine
  • (+)-5-iodo-2'-deoxyuridine
  • 5-iodo-2'-deoxyuridine
  • 5-iodo-2'-deoxyuridine
  • 5-iododeoxyuridine
  • 5-iododeoxyuridine
  • 5-iodouracil deoxyriboside
  • 5-iodouracil deoxyriboside
  • 5iudr
  • 5iudr
  • allergan
  • allergan 211
  • allergan 211
  • allergan-211
  • allergan-211
  • dendrid
  • dendrid
  • herplex
  • herplex
  • idox
  • idoxene
  • idoxuridin
  • idoxuridin
  • idoxuridin
  • idoxuridina
  • idoxuridina
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridine
  • idoxuridinum
  • idoxuridinum
  • idu
  • idu
  • idu
  • iododeoxyridine
  • iododeoxyridine
  • iododeoxyuridine
  • iododeoxyuridine
  • iododeoxyuridine
  • iodoxuridine
  • iodoxuridine
  • joddeoxiuridin
  • joddeoxiuridin
  • kerecid
  • kerecid
  • ophthalmadine
  • ophthalmadine
  • sk&f-14287
  • sk&f-14287
  • stoxil
  • stoxil
  • stoxil

Clinical trials

NCT IDPhaseStart dateSponsor(s)
NCT00003405Phase 2Apr 1, 1998National Cancer Institute (NCI), Rush University
NCT00109785Phase 1Mar 1, 1997Cornell University, National Cancer Institute (NCI)
Showing 2 of 2 trials
Page 1 / 1

Organizations

Research & Development (3)

OrganizationOrg typeTrialsAs lead sponsorPhasesEarliest year
National Cancer Institute (NCI)Government2021997
Cornell UniversityAcademic/Hospital1111997
Rush UniversityAcademic/Hospital1111998
3 organizations
Page 1 / 1

Marketing (5)

OrganizationOrg typeRelationshipDate
AlconFor profitNDA2Jun 28, 1963
AllerganFor profitNDA2Jun 11, 1963
AllerganFor profitNDAJun 11, 1963
GlaxoSmithKlineFor profitMKTGApr 6, 1964
GlaxoSmithKlineFor profitNDA2Apr 6, 1964