Cyclo Therapeutics Reports Full Year 2023 Financial Results and Provides Business Update
March 18 2024 - 9:05AM
Business Wire
Continued progress of pivotal Phase 3 study
(TransportNPC™) evaluating Trappsol® Cyclo™ for the treatment of
Niemann-Pick Disease Type C1 (NPC1) toward 48-week comparative
interim analysis data readout, planned for Q1 2025
Aligned development strategy for Trappsol®
Cyclo™ with FDA to enable a patient population lacking available
therapies to have earlier access to a potentially efficacious
product with an acceptable safety profile
Ended the year with approximately $9.2 million
cash to fund operations; continued efforts to bolster cash position
and extend runway through clinical and regulatory milestones
Cyclo Therapeutics, Inc. (Nasdaq: CYTH) (“Cyclo Therapeutics” or
the “Company”), a clinical stage biotechnology company dedicated to
developing life-changing medicines through science and innovation
for patients and families living with diseases, today reported its
financial results for the full year 2023 and provided a business
update.
“We made significant progress over the course of the past year.
We continue to be extremely active with the NPC patient and
scientific communities and believe these valuable interactions
underscore the progress we have seen with the advancement of our
TransportNPC study,” commented N. Scott Fine, Chief Executive
Officer of Cyclo Therapeutics. “Following the completion of the
merger with Applied Molecular Transport, we are poised to continue
building momentum and achieving the value-driving milestones ahead.
Importantly, supported with the positive feedback from FDA and
alignment on our strategy moving forward, we remain focused on
generating the appropriate data required to successfully drive our
TransportNPC study across the finish line and the potential to
provide a much-needed treatment option for the NPC community. We
are grateful for the continued support of our investors, including
Rafael Holdings and other longtime shareholders, who have bolstered
our cash runway and helped position us to achieve our mission and
continue our work to advance the clinical development of Trappsol®
Cyclo™.”
William Conkling, Chief Executive Officer of Rafael Holdings,
Inc., added, “We are pleased with the continued clinical progress
and operational execution and look forward to the continued
advancement of those efforts in 2024.”
Recent Highlights
- Granted U.S. patent covering use of Trappsol® Cyclo™ for
treatment of Alzheimer's Disease from the U.S. Patent and Trademark
Office;
- Completed merger with Applied Molecular Transport Inc to focus
on advancing Cyclo Therapeutics’ pivotal Phase 3 global study,
TransportNPC™, evaluating Trappsol® Cyclo™ for NPC;
- Dr. Caroline Hastings, Chair of the Company’s Phase 3 Trappsol®
Cyclo™ program steering committee and Global Principal Investigator
for the Company’s ongoing TransportNPC™ study presented at the 20th
Annual WORLDSymposium™; and
- Announced positive outcome from Type C Meeting with the U.S.
FDA discussing Trappsol® Cyclo™ clinical program for the treatment
of Niemann-Pick Disease Type C1.
- Strengthened Balance Sheet with early exercise of warrants by
board members, management and a significant shareholder resulting
in bolstered cash proceeds of $2.4 million. The Investors include
Rafael Holdings, Inc., a significant shareholder of the Company,
several directors of the Company, Company management, and their
affiliates.
Summary of Financial Results for the Full Year 2023
Net loss for the year ended December 31, 2023 was approximately
$20.1 million. Research and development expenses increased 58% to
$14.2 million for the year ended December 31, 2023, from $9.0
million for the year ended December 31, 2022. The changes in
research and development expenses resulted from the increased
activity in the Company’s Phase 3 study of Trappsol® Cyclo™ for the
treatment of NPC.
The Company ended the year with approximately $9.2 million of
cash.
About Cyclo Therapeutics
Cyclo Therapeutics, Inc. is a clinical-stage biotechnology
company dedicated to developing life-changing medicines through
science and innovation for patients and families living with
disease. The Company’s Trappsol® Cyclo™, an orphan drug designated
product in the United States and Europe, is the subject of four
formal clinical trials for Niemann-Pick Disease Type C1, a rare and
fatal genetic disease, (www.ClinicalTrials.gov NCT02939547,
NCT02912793, NCT03893071 and NCT04860960). The Company is
conducting a Phase 2b clinical trial using Trappsol® Cyclo™
intravenously in early Alzheimer’s disease (NCT05607615) based on
encouraging data from an Expanded Access program for Alzheimer’s
disease (NCT03624842). Additional indications for the active
ingredient in Trappsol® Cyclo™ are in development. For additional
information, visit the Company’s website:
www.cyclotherapeutics.com.
Safe Harbor Statement
This press release contains “forward-looking statements” about
the company’s current expectations about future results,
performance, prospects and opportunities, including, without
limitation, statements regarding the satisfaction of closing
conditions relating to the offering and the anticipated use of
proceeds from the offering. Statements that are not historical
facts, such as “anticipates,” “believes” and “expects” or similar
expressions, are forward-looking statements. These statements are
subject to a number of risks, uncertainties and other factors that
could cause actual results in future periods to differ materially
from what is expressed in, or implied by, these statements. The
factors which may influence the company’s future performance
include the company’s ability to obtain additional capital to
expand operations as planned, success in achieving regulatory
approval for clinical protocols, enrollment of adequate numbers of
patients in clinical trials, unforeseen difficulties in showing
efficacy of the company’s biopharmaceutical products, success in
attracting additional customers and profitable contracts, and
regulatory risks associated with producing pharmaceutical grade and
food products. These and other risk factors are described from time
to time in the company’s filings with the Securities and Exchange
Commission, including, but not limited to, the company’s reports on
Forms 10-K and 10-Q. Unless required by law, the company assumes no
obligation to update or revise any forward-looking statements as a
result of new information or future events.
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version on businesswire.com: https://www.businesswire.com/news/home/20240318041375/en/
Investor Contact: JTC Team, LLC Jenene Thomas (833)
475-8247 CYTH@jtcir.com
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