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Experimental: doxycycline

ANRS, Emerging Infectious Diseases · Phase 3 active Small molecule

Doxycycline inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit, preventing peptide bond formation.

Doxycycline inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit, preventing peptide bond formation. Used for Emerging infectious diseases (investigational indication under ANRS Phase 3 trial).

At a glance

Generic nameExperimental: doxycycline
SponsorANRS, Emerging Infectious Diseases
Drug classTetracycline antibiotic
TargetBacterial 30S ribosomal subunit
ModalitySmall molecule
Therapeutic areaInfectious Diseases
PhasePhase 3

Mechanism of action

Doxycycline is a tetracycline antibiotic that works by blocking bacterial protein synthesis through reversible binding to the bacterial 30S ribosomal subunit. This prevents the attachment of aminoacyl-tRNA to the ribosome, thereby inhibiting peptide chain elongation. The drug is bacteriostatic, meaning it stops bacterial growth rather than directly killing the organisms.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results