STOCK TITAN

Mereo BioPharma Regains Compliance with Nasdaq Minimum Bid Price Requirement

Rhea-AI Impact
(Low)
Rhea-AI Sentiment
(Neutral)
Tags
Rhea-AI Summary

Mereo BioPharma Group plc (NASDAQ: MREO) has regained compliance with Nasdaq's minimum bid price requirement. Following a notification on May 26, 2022, regarding non-compliance due to a closing bid price below $1.00 for 30 consecutive days, the company has successfully maintained a closing bid price of $1.00 or more for 10 consecutive business days, from June 17 to July 1, 2022. This achievement closes the matter with Nasdaq. Mereo focuses on innovative therapies for rare diseases and oncology, with products in clinical stages and significant partnerships.

Positive
  • Regained compliance with Nasdaq's minimum bid price requirement.
  • Successfully maintained a closing bid price of $1.00 or more for 10 consecutive days.
  • Focus on developing innovative therapies in rare diseases and oncology.
Negative
  • None.

LONDON and MOUNTAIN VIEW, Calif., July 05, 2022 (GLOBE NEWSWIRE) -- Mereo BioPharma Group plc (NASDAQ: MREO), (“Mereo” or “the Company”), a clinical-stage biopharmaceutical company focused on rare diseases and oncology, today announced that it has received a written notification (the “Notification Letter”) from the Listing Qualifications Department of the Nasdaq Stock Market, LLC (“Nasdaq”) informing the Company that it has regained compliance with the minimum bid price requirement set forth in Nasdaq Listing Rule 5450(a)(1) (the “Minimum Bid Price Requirement”) and the matter is closed.

As announced on May 26, 2022, the Company was notified by Nasdaq that it was not in compliance with the Minimum Bid Price Requirement, as the closing bid price of the Company's American Depositary Shares (the "ADSs") had been below US$1.00 for 30 consecutive business days. To regain compliance with the Minimum Bid Price Requirement, Mereo was required to maintain a minimum closing bid price of $1.00 or more for at least 10 consecutive business days.

The Notification Letter confirmed that the Company evidenced a closing bid price of the Company’s ADSs on Nasdaq at or greater than the $1.00 per ADS minimum requirement for the last 10 consecutive business days from June 17, 2022 to July 1, 2022 and that the Company has regained compliance with Minimum Bid Price Requirement.

About Mereo BioPharma
Mereo BioPharma is a biopharmaceutical company focused on the development of innovative therapeutics for rare diseases and in oncology and plans to commercialize selected rare disease programs. The Company has developed a portfolio of six clinical stage product candidates. The Company has two rare disease product candidates, setrusumab for the treatment of osteogenesis imperfecta (OI) and alvelestat for the treatment of severe Alpha-1 antitrypsin deficiency (AATD) and Bronchiolitis Obliterans Syndrome (BOS). The Company’s partner, Ultragenyx Pharmaceutical, Inc., has initiated a pivotal Phase 2/3 pediatric study in young adults (5-25 years old) for setrusumab in OI and expects to initiate a study in pediatric patients (2-5 years old) in the second half of 2022. The partnership with Ultragenyx includes potential milestone payments of up to $254 million and royalties to Mereo on Ultragenyx territories. Mereo has retained EU and UK commercial rights and will pay Ultragenyx royalties on those territories. Alvelestat has received U.S. Orphan Drug Designation for the treatment of AATD and positive top-line data were recently reported from a Phase 2 proof-of-concept study in North America, Europe and the UK. Mereo’s lead oncology product candidate, etigilimab (anti-TIGIT), is currently in an open label Phase 1b/2 basket study evaluating anti-TIGIT in combination with an anti-PD-1 in a range of tumor types. The Company’s second oncology product, navicixizumab, for the treatment of late line ovarian cancer, has completed a Phase 1 study and has been partnered with OncXerna Therapeutics, Inc. The global licensing agreement with OncXerna includes payments of up to $300 million in milestones and royalties. OncXerna has stated that they intend to initiate a Phase 3 trial of navicixizumab in late line ovarian cancer patients.

Forward-Looking Statements
This press release contains “forward-looking statements.” All statements other than statements of historical fact contained in this press release are forward-looking statements within the meaning of Section 27A of the United States Securities Act of 1933, as amended (the “Securities Act”), and Section 21E of the United States Securities Exchange Act of 1934, as amended (the “Exchange Act”). Forward-looking statements usually relate to future events and anticipated revenues, earnings, cash flows or other aspects of our operations or operating results. Forward-looking statements are often identified by the words “believe,” “expect,” “anticipate,” “plan,” “intend,” “foresee,” “should,” “would,” “could,” “may,” “estimate,” “outlook” and similar expressions, including the negative thereof. The absence of these words, however, does not mean that the statements are not forward-looking. These forward-looking statements are based on the Company’s current expectations, beliefs and assumptions concerning future developments and business conditions and their potential effect on the Company. While management believes that these forward-looking statements are reasonable as and when made, there can be no assurance that future developments affecting the Company will be those that it anticipates.

All of the Company’s forward-looking statements involve known and unknown risks and uncertainties some of which are significant or beyond its control and assumptions that could cause actual results to differ materially from the Company’s historical experience and its present expectations or projections. You should carefully consider the foregoing factors and the other risks and uncertainties that affect the Company’s business, including those described in the “Risk Factors” section of its latest Annual Report on Form 20-F, reports on Form 6-K and other documents furnished or filed from time to time by the Company with the Securities and Exchange Commission. The Company wishes to caution you not to place undue reliance on any forward-looking statements, which speak only as of the date hereof. The Company undertakes no obligation to publicly update or revise any of our forward-looking statements after the date they are made, whether as a result of new information, future events or otherwise, except to the extent required by law.

Mereo BioPharma Contacts:   
Mereo +44 (0)333 023 7300
Denise Scots-Knight, Chief Executive Officer  
Christine Fox, Chief Financial Officer  
  
Burns McClellan (Investor Relations Adviser to Mereo) +01 212 213 0006
Lee Roth  
Investors investors@mereobiopharma.com

FAQ

What does Mereo BioPharma's compliance with Nasdaq mean?

It means Mereo BioPharma has met the minimum bid price requirement to remain listed on the Nasdaq stock exchange.

When did Mereo BioPharma regain compliance with Nasdaq?

Mereo regained compliance on July 5, 2022, after maintaining a closing bid price of $1.00 or more for 10 consecutive business days.

What is Mereo BioPharma's stock symbol?

Mereo BioPharma's stock symbol is MREO.

What events led to Mereo BioPharma's notification from Nasdaq?

Mereo received a notification on May 26, 2022, for not complying with the minimum bid price requirement due to a closing bid price below $1.00.

What are Mereo BioPharma's main product focuses?

Mereo is focused on developing therapies for rare diseases and oncology.

Mereo BioPharma Group plc American Depositary Shares

NASDAQ:MREO

MREO Rankings

MREO Latest News

MREO Stock Data

487.16M
147.88M
1.02%
68.28%
3.63%
Biotechnology
Pharmaceutical Preparations
Link
United States of America
LONDON