Viridian Therapeutics to Webcast VRDN-001 Phase 3 THRIVE Topline Results on September 10, 2024
September 09 2024 - 4:01PM
Business Wire
- THRIVE global phase 3 clinical trial
evaluated efficacy and safety of VRDN-001 in patients with active
thyroid eye disease (TED) -
- Conference call and webcast to be held
Tuesday, September 10, at 8:00 a.m. ET -
Viridian Therapeutics, Inc. (NASDAQ: VRDN), a biopharmaceutical
company focused on discovering and developing potential
best-in-class medicines for serious and rare diseases, will host a
conference call and webcast to report topline data for the THRIVE
phase 3 clinical trial, evaluating VRDN-001 in patients with active
TED, on Tuesday, September 10, 2024 at 8:00am ET.
Conference call and webcast information
The webcast can be accessed under “Events and Presentations” on
the Investors section of the Viridian website at
viridiantherapeutics.com. To participate in the conference call,
please dial 800-715-9871 (domestic) or 646-307-1963 (international)
and reference code 8636908. A replay of the webcast will be
available following the completion of the event.
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. Viridian’s 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 Viridian’s product
candidates VRDN-001, VRDN-003, VRDN-006 and VRDN-008; clinical
trial designs, including the REVEAL-1 and REVEAL-2, global phase 3
clinical trials for VRDN-003; and Viridian’s product candidates
potentially being best-in-class.
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 Viridian’s product candidates; that
results or data from completed or ongoing clinical trials may not
be representative of the results of ongoing or future clinical
trials; that preliminary data may not be representative of final
data; the timing, progress and plans for our ongoing or future
research, preclinical and clinical development programs; changes to
trial protocols for ongoing or new clinical trials, including
adjustments that we may make to the VRDN-003 clinical trial designs
as a result of the VRDN-001 data; expectations and changes
regarding the timing for regulatory filings; regulatory
interactions expectations and changes regarding the timing for
enrollment and data; uncertainty and potential delays related to
clinical drug development; the duration and impact of regulatory
delays in our clinical programs; the timing of and our ability to
obtain and maintain regulatory approvals for our therapeutic
candidates; manufacturing risks; competition from other therapies
or products; estimates of market size; other matters that could
affect the sufficiency of existing cash, cash equivalents and
short-term investments to fund operations; our financial position
and projected cash runway; our future operating results and
financial performance; Viridian’s intellectual property position;
the timing of preclinical and clinical trial activities and
reporting results from same; and those risks set forth under the
caption “Risk Factors” in our most recent quarterly report on Form
10-Q filed with the Securities and Exchange Commission (SEC) on
August 8, 2024 and other subsequent disclosure documents filed with
the SEC. Any forward-looking statement speaks only as of the date
on which it was made. Neither the company, nor its affiliates,
advisors, or representatives, undertake any obligation to publicly
update or revise any forward-looking statement, whether as a result
of new information, future events or otherwise, except as required
by law. These forward-looking statements should not be relied upon
as representing the company’s views as of any date subsequent to
the date hereof.
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version on businesswire.com: https://www.businesswire.com/news/home/20240909312258/en/
Louisa Stone, 617-272-4604 Manager, Investor Relations
IR@viridiantherapeutics.com
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