Streptomycin

證據等級: L5 預測適應症: 10

目錄

  1. Streptomycin
  2. Streptomycin: From Bacterial Infections (Tuberculosis) to Conjunctivitis
    1. One-Sentence Summary
    2. Quick Overview
    3. Why is This Prediction Reasonable?
    4. Clinical Trial Evidence
    5. Literature Evidence
    6. US Market Information
    7. Safety Considerations
    8. Conclusion and Next Steps
    9. Disclaimer

## 藥師評估報告

Streptomycin: From Bacterial Infections (Tuberculosis) to Conjunctivitis

One-Sentence Summary

Streptomycin is a first-generation aminoglycoside antibiotic historically used to treat tuberculosis and other bacterial infections, though it is not currently marketed in this jurisdiction (0 registered licenses). The TxGNN model predicts it may be effective for Conjunctivitis, supported by 0 modern clinical trials and 20 pieces of literature, most dating from the 1940s–1950s era of early antibiotic use. Evidence is largely historical (field trials, case reports); no controlled modern studies exist for this specific indication.


Quick Overview

Item Content
Original Indication Not on file in regulatory data (0 licenses); historically used systemically for tuberculosis and other bacterial infections as a class-defining aminoglycoside
Predicted New Indication Conjunctivitis
TxGNN Prediction Score 99.87%
Evidence Level L3
US Market Status Not Marketed
Number of NDAs 0
Recommended Decision Hold

Why is This Prediction Reasonable?

Detailed, structured mechanism-of-action data (DrugBank MOA field) is not available for streptomycin in this evidence pack. However, the model’s own rationale confirms streptomycin’s well-established pharmacology: it is an aminoglycoside antibiotic that inhibits bacterial 30S ribosomal protein synthesis, producing bactericidal activity against a range of gram-negative and gram-positive organisms.

Bacterial conjunctivitis can be caused by many of the same pathogen classes streptomycin has historically targeted — including Haemophilus species, Brucella, Mycobacterium tuberculosis, and Francisella tularensis (the causative agent of tularemia-associated oculoglandular/Parinaud syndrome). This provides a plausible mechanistic bridge between streptomycin’s antibacterial spectrum and the proposed new indication.

That said, streptomycin is not the modern standard of care for ophthalmic infection. As the literature itself notes (PMID 3317953), streptomycin was the first aminoglycoside discovered (1943) but has since been clinically superseded in ophthalmology by newer aminoglycosides such as tobramycin and gentamicin, which have better local tolerability and safety profiles. The supporting evidence for streptomycin specifically in conjunctivitis is almost entirely from the 1940s–1950s (field trials in Morocco, experimental Hemophilus conjunctivitis studies, TB/Brucella case reports), predating modern trial design and safety standards.


Clinical Trial Evidence

Currently no related clinical trials registered for conjunctivitis.


Literature Evidence

PMID Year Type Journal Key Findings
13075256 1953 Field trial Rev Int Trachome Prophylaxis/treatment of seasonal conjunctivitis in rural Morocco via streptomycin and chloramine eye instillations, compared for effect
13075257 1953 Field trial Rev Int Trachome Prevention of seasonal conjunctivitis in southern Morocco: streptomycin eye-wash vs. aureomycin salve, comparative effects
18132879 1949 Historical clinical study Am J Ophthalmol Streptomycin effective in experimental conjunctivitis caused by Hemophilus sp.
15442493 1950 Case report La Semana Medica Primary tuberculous conjunctivitis with fistulized submaxillary adenopathy treated with systemic and local streptomycin
6789462 1981 Case report S Afr Med J Occupational Brucella keratoconjunctivitis treated with systemic tetracycline/co-trimoxazole/streptomycin plus topical chloramphenicol
5289718 1971 Laboratory study J Hygiene Streptomycin (and neomycin) effective at suppressing bacterial contamination during isolation of trachoma (TRIC) agent from conjunctival scrapings
38941282 2024 Case report Am J Case Rep Francisella tularensis causing Parinaud oculoglandular syndrome (granulomatous conjunctivitis) via conjunctival entry
19584516 2009 Case series/Review Indian J Med Microbiol Familial tularaemia cases, including oculoglandular (conjunctivitis) presentation
38298538 2023 Review Front Microbiol Review of tularemia treatment (experimental and clinical data); oculoglandular form frequently presents as conjunctivitis
3317953 1987 Review Surv Ophthalmol Historical review noting streptomycin as the first aminoglycoside (1943), superseded in ophthalmology by tobramycin/gentamicin

US Market Information

Streptomycin is not currently marketed in this jurisdiction — no NDA/license records are on file (0 total licenses).


Safety Considerations

Please refer to the package insert for safety information. Key warnings, contraindications, and drug-interaction data for streptomycin were not available in this evidence pack (flagged as a Blocking data gap — DG001: TFDA label warnings/contraindications must be obtained before any S1 safety evaluation can proceed).


Conclusion and Next Steps

Decision: Hold

Rationale: Evidence for streptomycin in conjunctivitis is limited to historical field trials and case reports from the 1940s–1950s (Evidence Level L3), with no modern controlled trials. Progression to a formal safety evaluation (S1) is also blocked by a missing TFDA label/warnings dataset (DG001, Blocking severity), and the drug is not currently marketed in this jurisdiction (0 licenses), which limits regulatory pathways for repurposing.

To proceed, the following is needed:

  • TFDA (or equivalent) package insert/label data — warnings, contraindications, DDI (DG001, Blocking)
  • Structured mechanism-of-action confirmation from DrugBank (DG002, High)
  • Modern comparative safety data given streptomycin’s known ototoxicity/nephrotoxicity profile relative to newer aminoglycosides already used ophthalmically (e.g., tobramycin)
  • Clarification of a viable regulatory pathway given the drug’s current non-marketed status

    Disclaimer

This content is for research purposes only and does not constitute medical advice. Clinical validation is required before any clinical application.



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