FDA Approves Likmez Metronidazole Oral Suspension 

Trichomoniasis Trichomonas vaginalis
Credit: CDC/Joe Miller.
Metronidazole is a nitroimidazole antimicrobial.

The Food and Drug Administration (FDA) has approved Likmez™, a ready-to-use liquid suspension formulation of metronidazole.

Likmez oral suspension is supplied in a 200mL bottle containing 500mg/5mL of metronidazole in a strawberry peppermint flavor. The product does not require refrigeration.

Likmez is indicated for the treatment of:

  • Symptomatic trichomoniasis caused by Trichomonas vaginalis in adult females and males when the diagnosis is confirmed.
  • Asymptomatic trichomoniasis caused by Trichomonas vaginalis in adult females when the organism is associated with endocervicitis, cervicitis, or cervical erosion.
  • Acute intestinal amebiasis (amoebic dysentery) and amebic liver abscess in adults and pediatric patients.
  • Serious infections caused by susceptible anaerobic bacteria in adults.

“Difficulty swallowing tablets and capsules should not be a barrier to accessing appropriate antibiotic therapy,” said Don Cilla, PharmD, MBA, Appili’s President and CEO. “Likmez provides a convenient alternative for patients who have difficulty taking solid oral medicines.”

References:

Appili Therapeutics announces US FDA approval of Likmez™ (ATI-1501) Metronidazole Oral Suspension. News release. Appili Therapeutics. September 25, 2023. Accessed September 26, 2023. https://www.businesswire.com/news/home/20230925938803/en/Appili-Therapeutics-Announces-U.S.-FDA-Approval-of-LIKMEZ%E2%84%A2-ATI-1501-Metronidazole-Oral-Suspension.