Ovoca Bio PLC Update on Completion Timelines for Phase II Study (3213C)
June 12 2023 - 1:00AM
UK Regulatory
TIDMOVB
RNS Number : 3213C
Ovoca Bio PLC
12 June 2023
Ovoca Bio plc
("Ovoca" or the "Company")
Ovoca Bio Provides Update on Completion Timelines for Phase II
Dose Ranging Study Assessing Orenetide for HSDD
Dublin, Ireland, 12 June 2023 - Ovoca Bio, a biopharmaceutical
company with a focus on women's health, today announces an update
regarding the completion timeline of its ongoing Phase II dose
ranging study assessing Orenetide (the "Study"), a novel treatment
for women with hypoactive sexual desire disorder ("HSDD"), which is
being conducted in Australia and New Zealand. The Company has been
informed by its retained Australian Contract Research Organisation
(CRO) that, due to issues with staffing levels at the CRO, the
timeline for delivery of the results of the Study has been delayed,
with the results now anticipated to be finalized in August as
opposed to the previously anticipated timeframe of June this year.
While this is disappointing, the staffing issues have now been
resolved and Ovoca wishes to assure its stakeholders that every
effort is being made to expedite the completion and ensure the
accuracy and reliability of the results of the Study.
Dr. Daniil Nemenov, SVP for Clinical Development &
Operations at Ovoca, expressed the company's position regarding the
delay, stating, "the team here at Ovoca believe the results of this
Study are of great significance to our stakeholders, patients, and
the broader medical community. Our team has been working diligently
with the CRO to address the challenges encountered, and we remain
committed to completing the Study in the most efficient and
accurate manner possible."
Ovoca would like to emphasize that this delay does not impact
the overall commitment and dedication towards advancing Orenetide
research and delivering therapeutic solution to patients. The
Company's primary focus remains on ensuring patient wellbeing,
adhering to rigorous scientific approach, and maintaining the
highest standards of quality throughout the Study.
Ovoca will keep shareholders updated should there be any further
developments or changes in respect of the revised timeline and the
Company looks forward to sharing the results of the Study in due
course.
End
For further information:
Ovoca Bio plc
Kirill Golovanov (Chief Executive)
Tel +353 1 661 9819
info@ovocabio.com
Davy (Nominated Adviser, Euronext Growth Listing Sponsor and
Broker)
Ivan Murphy / Daragh O'Reilly
Tel: +353 1 679 6363
About Ovoca Bio
Ovoca Bio is a European-based biopharmaceutical company with a
focus on women's health. The Company is currently developing a
novel treatment for women with hypoactive sexual desire disorder
(HSDD), a condition characterized by a distressing lack or loss of
sexual desire affecting an estimated 4 million premenopausal women
in the US alone.
The Company's lead product, Orenetide (earlier - BP-101), a
novel synthetic peptide administered through a nasal spray, is
clinically validated, with earlier conducted regional Phase II and
Phase III studies demonstrating statistically significant
improvement in a number of key efficacy outcomes, including an
increase in female sexual desire and reduction of symptoms of
distress associated with HSDD.
Ovoca Bio is seeking to develop the drug for major global
markets - in particular the United States and Europe.
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END
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