About Viridian Therapeutics
Viridian is a biopharmaceutical company focused on engineering and developing potential
best-in-class medicines for patients with serious and rare diseases. Viridians expertise in antibody discovery and protein engineering enables the development of
differentiated therapeutic candidates for previously validated drug targets in commercially established disease areas.
Viridian is advancing multiple
candidates in the clinic for the treatment of patients with thyroid eye disease (TED). The company is conducting a pivotal program for VRDN-001, including two global phase 3 clinical trials (THRIVE and THRIVE-2), to evaluate its efficacy and safety in patients with active and chronic TED. Viridian is also advancing VRDN-003 as a potential best-in-class subcutaneous therapy for the treatment of TED, including two planned global phase 3 clinical trials, REVEAL-1 and
REVEAL-2, to evaluate the efficacy and safety of VRDN-003 in patients with active and chronic TED.
In addition to its TED portfolio, Viridian is advancing a novel portfolio of neonatal Fc receptor (FcRn) inhibitors, including
VRDN-006 and VRDN-008, which has the potential to be developed in multiple autoimmune diseases.
Viridian is based in Waltham, Massachusetts. For more information, please visit www.viridiantherapeutics.com. Follow Viridian on LinkedIn and
X.
Forward Looking Statements
This press
release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of words such as, but not limited to, anticipate, believe,
continue, could, estimate, expect, intend, may, might, on track, plan, potential, predict, project,
design, should, target, will, or would or other similar terms or expressions that concern our expectations, plans and intentions. Forward-looking statements are neither historical facts nor
assurances of future performance. Instead, they are based on our current beliefs, expectations, and assumptions. Forward-looking statements include, without limitation, statements regarding: preclinical and clinical development of Viridians
product candidates VRDN-001, VRDN-003, VRDN-006 and VRDN-008; anticipated start dates of
studies, including the initiation date of the REVEAL-1 and REVEAL-2, global phase 3 clinical trials for VRDN-003; milestones;
timelines; anticipated data results and timing of their disclosure, including topline results; regulatory interactions and anticipated timing of regulatory submissions, including the anticipated IND submission for
VRDN-006 and the anticipated BLA submission for VRDN-001; Viridians expectation that its data package will support a BLA submission for VRDN-001 in the second half of 2025, pending data; Viridians expectation that its data package will support a marketing authorization application in Europe for VRDN-001;
clinical trial designs, including the REVEAL-1 and REVEAL-2, global phase 3 clinical trials for VRDN-003; Viridians plans
to launch VRDN-003 with a commercially available auto-injector pen, if approved; the potential utility, efficacy, potency, safety, clinical benefits, clinical response, convenience and number of indications of
VRDN-001, VRDN-003, VRDN-006 and VRDN-008; Viridians product candidates potentially
being best-in-class; and that Viridians cash, cash equivalents and short-term investments will be sufficient to fund its operations into the second half of 2026.
New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. No representations or warranties
(expressed or implied) are made about the accuracy of any such forward-looking statements. Such forward-looking statements are subject to a number of material risks and uncertainties including but not limited to: potential utility, efficacy,
potency, safety, clinical benefits, clinical response and convenience of Viridians product candidates; that results or data from completed or ongoing clinical trials may not be representative of the results of ongoing or future
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