
Memento Medicines launches with $93 million Series A to advance Tie2-activating bispecific for retinal disease
Key Takeaways
- Financing supports IND-enabling studies for MMT-205, with first-in-human studies anticipated in 2027.
- Exclusive worldwide license from MabTics and Curacle included upfront cash plus equity consideration for the Korean partners.
The newly formed biotech will use the financing to push MMT-205, a bispecific antibody that directly activates Tie2 while inhibiting VEGF, toward IND-enabling studies, with first-in-human trials slated for 2027.
Memento Medicines, a privately held biotech developing biologic therapies for retinal disease, has launched with a $93 million Series A round co-led by Forbion, RA Capital Management, and Avego BioScience Capital. Alongside the launch, the company secured worldwide rights for MMT-205 through an exclusive license agreement with South Korea–based MabTics Co., Ltd. and Curacle Co., Ltd.
MMT-205, previously known as MT-103, is a bispecific antibody designed to activate the Tie2 receptor while simultaneously inhibiting VEGF—two targets with a well-established role in the pathogenesis of retinal vascular disease. According to the company, proceeds from the financing will fund IND-enabling studies, with clinical trials expected to begin in 2027. Under the licensing terms, MabTics and Curacle received upfront cash and equity in Memento.
The arrival of faricimab (Vabysmo; Genentech), the
That distinction is the crux of the company's differentiation pitch. Memento says MMT-205 produces greater Tie2 activation and improved retinal vascular integrity than current therapies in preclinical models.
"MMT-205 holds the potential to become a best-in-class biologic therapy in nAMD and DME and is supported by a robust preclinical data package established by our partners at MabTics and Curacle," said Naveen Daryani, CEO of Memento Medicines, in a press release. He added that the investor syndicate's "deep domain expertise in ophthalmology" should help accelerate the program toward patients.
Dmitrij Hristodorov, PhD, general partner at Forbion, framed the asset in similar terms, calling MMT-205 a potentially "transformative therapeutic in retinal diseases" and pointing to the firm's track record building ophthalmology companies. For MabTics and Curacle, the deal validates a bispecific discovered in Korea on the global stage; the 2 companies continue to collaborate on biologics targeting vascular dysfunction, with Curacle separately advancing the small molecule Rivasterat (CU06) in phase 2 for DME.
The launch echoes the
The structure behind Memento reinforces the asset-centric thesis driving much In connection with the financing, Hristodorov, Zach Scheiner, PhD (RA Capital), Vishal Kapoor, MBA (Avego BioScience Capital), and Megan Krench, PhD (Sanofi Ventures), will join Memento's board of directors.
Whether MMT-205's direct-agonism approach translates into a durability or drying advantage over an entrenched standard of care will not be clear until clinical data arrive late this decade. For now, Memento has the capital, the syndicate, and a mechanistic story distinct enough to earn a close look from the retina community.
References:
Memento Medicines Launches with $93 Million Series A Financing to advance Tie2 Agonist and VEGF Inhibitor Bispecific Antibody Therapy for Retinal Diseases. Published June 18, 2026. Accessed June 22, 2026.
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