Lead development candidate, AMP-410, leverages proprietary Ampersand technology to block VEGF and allosterically activate 4-1BB signaling – unlike traditional bispecific molecules – driving both adaptive and innate anti-tumor activity
In multiple preclinical models of hard-to-treat cancers, AMP-410 showed strong efficacy when compared to four other clinical-stage immunotherapies, including an anti-VEGF/PD-1 bispecific antibody; IND-enabling studies to begin this year
AMP-410 was discovered and designed by Ampersand’s Address, Navigate, Determine (AND
BOSTON, April 28, 2025 (GLOBE NEWSWIRE) — Ampersand Biomedicines, a multi-product platform company developing smarter medicines that act specifically at the site of disease and nowhere else, today announced preclinical data for one of its lead development candidates, AMP-410, a novel potential first-in-class bifunctional anti-VEGF/4-1BB AND-Body
AMP‑410 was discovered and developed using the Ampersand platform to block VEGF, which then triggers allosteric activation of the 4‑1BB pathway selectively in tumors. This novel molecular mechanism is different from other bispecific molecules, and reprograms the tumor microenvironment with potent activation of both adaptive and innate immune responses and minimal systemic activity. AMP-410 was evaluated in multiple preclinical models of hard-to-treat cancers, including melanoma, colorectal, and lung cancer. Findings show that AMP-410 induced more durable anti-tumor immunity compared to four other classes of clinical immunotherapies. Notably, AMP-410 showed initial promising monotherapy efficacy compared to an anti-VEGF/PD-1 bispecific antibody in a non-small cell lung cancer (NSCLC) model, demonstrating its potential to treat tumors resistant to checkpoint inhibitors. AMP-410 monotherapy achieved 90% tumor-free survival in colorectal cancer and extended survival in melanoma models; when combined with anti-PD-1, it drove 100% tumor-free survival in colorectal cancer and further extended survival in melanoma. Additional mechanistic data demonstrate that the AND-Body’s unique bifunctional targeting and activity mechanisms not only enhanced immune cell infiltration of the tumor and prevented T cell exhaustion, but also led to durable anti-tumor immunity and improved tolerability.
“Our Address, Navigate, Determine (AND)
Poster presentation details:
Title: Anti-VEGF/4-1BB bifunctional AND-Body combines VEGF blockade and allosteric 4-1BB mechanism for sustained activation of adaptive and innate anti-tumor immunity
Poster Number: 4794/30
Session Date/Time: Tuesday, April 29, 9:00 a.m. – 12:00 p.m. CDT
About Ampersand Biomedicines
Ampersand Biomedicines enables a new way of programming medicines that work precisely where needed in the body and nowhere else. The company’s computationally powered Address, Navigate, Determine (AND)
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