DWTI announced before the open on 9/25 that the US FDA (Food and Drug Administration) has granted marketing approval for DW-5LBT (lidocaine patch, trade name Bondlido), as a treatment for neuropathic pain after shingles (post- herpetic neuralgia) in adults, jointly developed with MEDRx (4586 TSE Growth).
Earlier this week on Monday 9/22, DWTI announced that the FDA had conditionally approved a change in the trade name from “Lydolyte” to “Bondlido” (the FDA had requested a name change to avoid confusion with an existing product).
Preparations for the launch will be made, including the selection of sales partners, with sales planned to begin in the US in the first half of 2026.
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