ABOUT
Broadening the potential of long-acting HIV maintenance
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.
PROOF POINTS
We are doing a couple of things you might be interested in
94%
Maintained HIV-1 RNA below 50 copies/mL through Week 24 in Phase 2a
0
Virologic failures among Phase 2a study completers
Q2M
Every-two-month dosing evaluated in Phase 2a and Phase 2b
PHASE 2B
Enrollment completed; interim analysis expected by year-end 2026
Long-acting HIV is not one-size-fits-all
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.
Applicability How many patients can realistically access and remain on a treatment matters as much as how often it is dosed. Treatment complexity Comorbidities and polypharmacy can add significant complexity to lifelong HIV management, increasing the importance of regimen design and DDI considerations. Clinical flexibility The future of long-acting care is likely to include multiple dosing and delivery options tailored to different patient needs rather than a single universal interval.
Biologics development experience that extends beyond our own pipeline
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.
Formulation Development
cGMP Manufacturing
Analysis and Analytical Method Development
Regulatory Affairs

