Lakefront Biotherapeutics discloses six weeks of share buybacks through July 31
The company reported repurchasing nearly 588,000 shares for about €15.1 million since late June under a program announced June 9, 2026.
SEC filing (6)
The company reported repurchasing nearly 588,000 shares for about €15.1 million since late June under a program announced June 9, 2026.
SEC filing (6)
The company now pegs one-time severance costs at $6.2 to $7.5 million after saying in June it could not yet quantify the expense.
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Lisata Therapeutics slashed staff and lost its R&D chief on August 3, 2026, while suing Kuva Labs over an alleged breach of their merger agreement.
SEC filing
The company reported a wider net loss and cut its full-year revenue outlook to €1.6–1.9 billion while confirming Oelkers will succeed Ugur Sahin by February 2027.
SEC filing (2)
Johnson & Johnson said Jennifer Taubert is stepping down after more than two decades at the company, with Tom Cavanaugh taking over effective September 1, 2026.
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The appointment took effect August 1, 2026, and Gilson brings prior CFO and equity research experience in biotech to the role.
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The amendment gives Evolus exclusive rights to sell the HA gel line in three more markets, with commercialization targeted for 2028.
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More than 400 patient start forms were filed for IMCIVREE in acquired hypothalamic obesity as RM-718 posted early efficacy data in the same disease.
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The designation gives CervoMed early, coordinated access to UK regulatory, health system, and reimbursement bodies as it seeks a partner for a planned Phase 3 trial.
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A Curium merger unit will merge into Lantheus, which survives as Curium's subsidiary, with holders getting $102.50 cash plus CVRs worth up to $12.00.
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The companies will combine into Supernus, Inc., a CNS-focused biopharmaceutical company, with closing expected in the fourth quarter of 2026.
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The company reported second-quarter 2026 results on August 3 and lifted its full-year revenue and profitability targets while its planned merger with Supernus is expected to close in the fourth quarter.
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The company reported a May 2026 Type C meeting confirmed its SOL-1 trial with confirmatory evidence is sufficient for a wet AMD submission, and posted $598.6 million in cash as of June 30, 2026.
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The company reported VYJUVEK sales growth, described progress on European launches, and set timelines for several ophthalmology, respiratory, dermatology, and oncology programs.
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Autolus drew a $75 million first tranche on July 30, 2026, with up to $175 million more available across three additional tranches tied to revenue milestones.
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The company posted preliminary Q2 net product revenue and lined up a five-year credit facility with Perceptive Advisors as it raised full-year sales guidance.
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Vertex lifted its full-year revenue outlook and disclosed a November 30 FDA decision date for povetacicept in IgA nephropathy while confirming plans to close its Crinetics acquisition in the third quarter.
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The company said cash of $427.3 million should fund operations into 2029 as it advances GlyphAllo and GlyphAgo through mid-stage trials.
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The company closed the first tranche of a Series D preferred stock deal with an affiliate and told Nasdaq its board no longer has a majority of independent directors.
SEC filing
Chairman Anthony Giovinazzo left the board on July 31 while independent director Depesh Narotam joined effective July 27, 2026.
SEC filing (2)
The August 3, 2026 prospectus supplement replaces a prior offering under which Stoke had already sold about 4.7 million shares for $146.4 million in net proceeds.
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Keros initiated its Phase 2 trial of rinvatercept in Duchenne muscular dystrophy and still expects initial data in the first half of 2027, while cash fell to $257.6 million.
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Moleculin Biotech priced a public offering of common stock, pre-funded warrants, and common warrants, with share delivery expected around August 3, 2026.
SEC filing (2)
The Boston biotech said Ahlers, a longtime life sciences finance executive, took the CFO role effective July 30, 2026, with a base salary of $450,000.
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The company reported $118.4 million in fiscal third-quarter revenue and raised its fiscal 2026 revenue outlook to $456-$457 million.
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Supernus announced a definitive all-stock merger of equals with Indivior on the same day it posted 32% revenue growth and raised full-year guidance.
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Indivior will absorb Supernus in a stock-for-stock deal that renames the combined company and pays holders a $1 billion special dividend.
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The company raised its full-year 2026 revenue targets and reported positive Phase 3 data supporting a simplified BRIUMVI dosing regimen.
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The company said neither departure stemmed from a disagreement over its operations, policies, or practices.
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Crinetics disclosed the Vertex merger agreement, an FDA rare pediatric disease designation for atumelnant, and PALSONIFY sales growth in its second-quarter update.
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BioLife Solutions filed an 8-K on August 3, 2026 disclosing a video message from Repligen's CEO to BioLife employees about the companies' planned merger.
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The biopharmaceutical company expanded its board to five members, adding a former Johnson & Johnson licensing and M&A executive effective August 3, 2026.
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The combined company begins trading as OBX on Nasdaq August 4, 2026, with cash expected to fund operations into the second half of 2028.
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ORIC reported second quarter 2026 results with the Himalayas-1 prostate cancer trial underway, a darolutamide supply pact with Bayer, and cash guided into second half 2028.
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The board added the President title, approved compensation and equity awards, and named Jackson a director, all effective August 1, 2026.
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The company appointed Dr. Faiçal Miyara as CBO and Jim Ziegler as CCO on August 2, 2026, dividing global deal-making from U.S. and ex-China commercial duties.
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The offering priced shares and warrants at $0.75 apiece, with proceeds earmarked for Annamycin development and working capital.
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Stoke Therapeutics said its Phase 3 EMPEROR trial in Dravet syndrome finished enrolling 162 patients, with a data readout expected in the third quarter of 2027 and a rolling NDA submission targeted to begin in early 2027
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The plan, adopted without stockholder approval under Nasdaq inducement rules, is limited to new hires as an incentive for joining the company.
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The company is adjusting its Friedreich ataxia trial after early data and has begun dosing in a new myotonic dystrophy study, with $207.4 million in cash on hand.
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FDA cleared CASGEVY for children as young as 2, and the company began Phase 1 trials for CTX340 and CTX460 while cash stood at $2,364.4 million.
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Jazz reported record quarterly revenue of $1.2 billion and set up a possible near-term launch of Ziihera in a new gastric cancer indication.
SEC filing