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Mereo BioPharma Group plc (MREO) reports it has received a second notice from Nasdaq that its American Depositary Shares remain below the $1.00 per share minimum bid price required for continued listing on the Nasdaq Capital Market. The company has been granted an additional 180-day compliance period, until February 16, 2027, to meet this Bid Price Requirement by achieving a closing bid of at least $1.00 for 10 consecutive business days. If compliance is not regained by that date, Nasdaq staff will move to delist the securities, though Mereo would be able to appeal to a Nasdaq Hearings Panel. The company states that the notices have no immediate effect on trading and that it will continue monitoring its share price and may consider options to regain compliance.
EcoR1 Capital, LLC, Oleg Nodelman and EcoR1 Capital Fund Qualified, L.P. report beneficial ownership of Mereo BioPharma Group plc Ordinary Shares. EcoR1 and Nodelman each report beneficial ownership of 5,000,000 Ordinary Shares, while the Qualified Fund reports 4,732,750 Ordinary Shares, each representing 0.6% of the outstanding class based on 798,093,044 Ordinary Shares outstanding as of May 11, 2026. The position is held through American Depositary Shares, with 1,000,000 ADS representing 5,000,000 Ordinary Shares and 946,550 ADS representing 4,732,750 Ordinary Shares. The filers state the holdings are not for the purpose of changing or influencing control of Mereo BioPharma and disclaim group status and beneficial ownership beyond their pecuniary interest.
Mereo BioPharma Group plc reported a six‑month 2026 net loss of $13.7 million, an improvement from $27.5 million a year earlier, with no product revenue and operating expenses focused on rare‑disease programs setrusumab and alvelestat. Cash and cash equivalents were $30.1 million at June 30, 2026, versus $56.1 million at June 30, 2025, supporting management’s expectation that current resources will fund operations into late 2027.
Research and development spending fell to $6.6 million for the first half from $9.3 million, and general and administrative expenses declined to $9.2 million from $12.8 million, reflecting delayed and reduced pre‑commercial and development activities. Foreign currency movements contributed a $1.3 million gain versus an $8.1 million loss in the prior‑year period.
As a subsequent event, Mereo entered an option and license agreement with Sentynl Therapeutics granting U.S. commercial and global manufacturing rights to alvelestat. On option exercise, Mereo would be eligible for $40 million in upfront and R&D payments, up to $435 million in milestones, and double‑digit tiered U.S. royalties, while leading the global Phase 3 study.
Mereo BioPharma Group plc reported second-quarter 2026 results, highlighting a smaller net loss and an extended cash runway alongside key partnering progress. Net loss for the quarter was $7.0 million, improving from $14.6 million a year earlier, driven mainly by sharply lower research and development spending.
As of June 30, 2026, cash and cash equivalents were $30.1 million, which the company expects will fund operations into late 2027. Mereo entered an option and license agreement with Sentynl Therapeutics for alvelestat, with eligibility for $40 million in upfront and R&D payments on option exercise, up to $435 million in milestones, and double-digit tiered U.S. royalties. For setrusumab, two Phase 3 studies in osteogenesis imperfecta did not meet primary fracture endpoints but showed statistically significant gains in bone mineral density and other measures, and Mereo and Ultragenyx are in regulatory discussions on a potential path forward.
Mereo BioPharma Group plc entered into an Option and License Agreement with Sentynl Therapeutics for the U.S. commercial and global manufacturing rights to alvelestat for alpha-1 antitrypsin deficiency-associated lung disease (AATD-LD). The agreement grants Sentynl an exclusive option to license U.S. commercialization rights while Mereo retains commercial rights for the rest of the world.
Under the terms, Mereo will receive a non-refundable option fee and, upon option exercise, would be eligible for $40 million in upfront and R&D payments, up to $435 million in potential regulatory and commercial milestones, and double-digit tiered royalties on U.S. net sales. Sentynl would also fund the alvelestat Phase 3 development program on option exercise. Mereo will lead the global Phase 3 study and regulatory interactions until completion, while the companies collaborate during a short option period to refine the Phase 3 design and advance manufacturing.
Mereo BioPharma Group plc ownership disclosure: EcoR1 Capital, LLC, EcoR1 Capital Fund Qualified, L.P. and Oleg Nodelman jointly report beneficial ownership on an amendment to Schedule 13G/A. The filing shows EcoR1 and Mr. Nodelman each report shared voting and dispositive power over 66,844,275 Ordinary Shares (representing 8.4% of the class). The Qualified Fund reports shared voting and dispositive power over 62,644,610 Ordinary Shares (representing 7.8%).
The filing states these Ordinary Shares are held through 13,368,855 American Depositary Shares (each ADS = 5 Ordinary Shares) and that the percentage calculations use 798,078,829 Ordinary Shares outstanding as of March 18, 2026 as reported in the issuer's Form 10-K for the fiscal year ended December 31, 2025. The reporting persons disclaim group membership and assert the holdings were not acquired to change control.
Mereo BioPharma Group plc ownership filing shows Bank of America Corporation reports beneficial ownership of 40,976,460 ordinary shares, representing 5.1% of the class. The calculation cites 798,078,829 shares outstanding as of March 18, 2026 from the issuer's Form 10-K. The filing states that the reported holdings reflect shared voting and dispositive power across Bank of America and certain wholly owned subsidiaries.
Mereo BioPharma Group plc reported the results of its 2026 Annual General Meeting, where all resolutions passed. Shareholder turnout was high, with 436,766,255 ordinary shares represented in person or by proxy.
Shareholders adopted the annual report and accounts for the year ended December 31, 2025, with 98.29% of votes cast in favor, and re-appointed PricewaterhouseCoopers LLP as auditors with 98.59% support. The Audit and Risk Committee was authorized to determine PwC’s remuneration.
Investors approved the directors’ remuneration report with 93.35% support and the directors’ remuneration policy, effective after the AGM, with 91.74% support. The compensation of named executive officers received 91.71% advisory approval. Justin Roberts, Dr. Daniel Shames and Marc Yoskowitz were each re-elected as directors, receiving around 94% of votes cast.
Shareholders also authorized the directors to allot shares and grant rights to subscribe or convert up to a maximum nominal amount of £3,591,354.73, and to do so on a non-pre-emptive basis, both authorities running until June 30, 2029. These replace earlier share issuance authorities to the extent not already used.
Mereo BioPharma Group plc filed an amended report to correct a technical item tag and reiterated its first quarter 2026 results and clinical updates. The company reported a net loss of $6.7 million for the quarter, improving from $12.9 million a year earlier, as operating loss narrowed and foreign currency gains increased.
Research and development expenses rose to $4.7 million, mainly from higher setrusumab costs, while general and administrative expenses fell to $4.0 million driven by ADR reimbursement and lower pre-commercial spending. Cash and cash equivalents were $36.2 million as of March 31, 2026, which the company expects to fund operations into mid-2027.
Clinically, neither of the two global Phase 3 studies of setrusumab in osteogenesis imperfecta met their primary fracture-rate endpoints, though both achieved strong results on key secondary measures such as bone mineral density and vertebral fractures. Mereo and partner Ultragenyx have started discussions with regulators on a potential pediatric path. Mereo is also preparing alvelestat for a single Phase 3 trial in AATD lung disease and expects its partner āshibio to start a Phase 2 vantictumab trial in ADO2 in the second half of 2026.