Process Development
TMB-365/380 is being developed as a complete, antibody-only maintenance regimen for virologically suppressed adults. Its complementary host-and-virus targeting strategy is designed to support durable disease control while reducing small-molecule backbone complexity and exploring the potential for broader real-world applicability.94% | Maintained HIV-1 RNA below 50 copies/mL through Week 24 in Phase 2a0 | Virologic failures among Phase 2a study completersQ2M | Every-two-month dosing evaluated in Phase 2a and Phase 2bPHASE 2B | Enrollment completed; interim analysis expected by year-end 2026
Fewer doses can matter, but meaningful innovation in HIV maintenance therapy depends on more than dosing interval alone. As people with HIV live longer and care becomes more complex, the field must also consider efficacy, safety, treatment eligibility, polypharmacy and drug-drug interactions, resistance, clinical flexibility, and fit with ongoing care. TaiMed is developing antibody-based approaches with these realities in mind.
TaiMed's biologics development and manufacturing capabilities support both our internal programs and selected external partners. Our CDMO team provides integrated services across process development, analytical development, formulation, cGMP manufacturing, and regulatory support.