Latigo Biotherapeutics prices IPO at $18 per share on Nasdaq
The clinical-stage pain drug developer sold 19.2 million shares to raise about $315.7 million in net proceeds ahead of an August 10, 2026 closing.
SEC filing
The clinical-stage pain drug developer sold 19.2 million shares to raise about $315.7 million in net proceeds ahead of an August 10, 2026 closing.
SEC filing
The clinical-stage oncology company will sell 9,375,000 shares on Nasdaq under the ticker BLSM, with shares expected to begin trading around August 10, 2026.
SEC filing
Entera raised $275 million in a private placement led by BVF Partners to fund a registrational Phase 3 trial of its oral osteoporosis drug EB613 through NDA submission.
SEC filing
Cash stood at $88.8 million as of June 30, 2026, with runway guidance into 2029 as multiple retinal gene therapy programs move toward clinic.
SEC filing
The company said FDA talks clarified elements of the planned trial design, while it reported second-quarter 2026 results and a patent allowance for zervimesine.
SEC filing
Wetteny Joseph, the outgoing CFO, will stay on as a special advisor to the CEO through early 2027 under a transition agreement.
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The company said start-up activities for its Phase 2/3 acute kidney injury trial of Gemini continue, with enrollment targeted to begin by year-end.
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The Miramar, Florida biotech disclosed a Regulation D offering with a first sale date of July 29, 2026, sold in full to four investors.
SEC filing
The company closed the Breathe Right and LaCorium Health deals and lifted its revenue and EPS guidance for the year to account for them.
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Cartesian says AURORA Phase 3 data in MG are expected in early 2027, with a new in vivo partnership and $150 million credit facility extending cash runway into 2028.
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Enrollment continues in JANX007, JANX014, and JANX011 trials, with JANX013 still set to start clinical testing in the second half of 2026.
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Viatris lifted full-year guidance midpoints, won FDA approval for a new contraceptive patch, and agreed to sell Tyrvaya rights to Harrow as it navigates manufacturing disruptions in India.
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Cullinan says a positive FDA meeting clears the way for a registrational AML study this quarter, with cash runway into 2029.
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SIGA said second-quarter TPOXX deliveries completed the last procurement order under its 19C contract with the U.S. strategic national stockpile.
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The company also named Ruth Perkins as incoming CFO and lowered its 2026 revenue and adjusted EBITDA guidance, citing currency and China softness.
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Lantheus reported second-quarter revenue of $388.2 million and said it is suspending its 2026 outlook as it awaits closing of its acquisition by Curium US Holdings.
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The regenerative medicine company entered an ATM sales agreement with BTIG and Citizens JMP on August 6, 2026, as shares traded near $2.37.
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Agenus reported second-quarter 2026 results and said dosing in its planned Phase 3 ROBBIN trial is expected to begin in early 2027, supported by a private placement completed in July.
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The company will issue the shares on or about August 6, 2026 to satisfy amounts owed under a secured note issued to Leonite in June 2026.
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Verrica posted record YCANTH dispensing volume in Q2 2026 and said its new $27.5 million credit facility could stretch cash into 2028.
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Climb Bio said it plans to present initial CLYM116 Phase 1 data on September 3, 2026 and expects Phase 2 dosing in IgA nephropathy to begin in the third quarter of 2026, with cash extending into the second half of 2028.
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The Phase 4 study will test LUPKYNIS alongside belimumab, obinutuzumab or anifrolumab in about 150 patients as Aurinia reports second-quarter results and reiterates 2026 revenue guidance.
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Sanuwave pulled its full-year outlook citing Medicare payment uncertainty as Q2 revenue fell 3% to $9.7 million and system sales dropped on reimbursement pressure and a used-equipment market.
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Second-quarter revenue fell 58% amid a slower-than-expected market recovery, prompting a lower full-year guidance range and continued cash burn.
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The company said its Phase 3 TEBE-AM trial is nearing its 540-patient enrollment target, with topline data possible by the end of 2026.
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Avalo also detailed a new anti-IL-1β antibody, AVTX-010, with an IND filing targeted for the first half of 2027, and reported $472.2 million in cash.
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Company says Phase 3 decision on cystic fibrosis candidate ARCT-032 is expected in Q4 2026, while ARCT-810 dosing has finished with data due later this quarter.
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Tiziana Life Sciences said CEO Ivor Elrifi bought company stock on Nasdaq on August 4 and August 6, 2026, each time at $1.00 per share.
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The company also flagged a fourth-quarter 2026 NDA resubmission for Zynquista and reported $190.6 million in cash and investments as of June 30, 2026.
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Aligos said its Phase 2 B-SUPREME study of pevifoscorvir sodium has finished enrolling patients, with topline data expected in late Q3 2027, as partner Amoytop advances an HBV antisense program in China.
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The company raised over $200 million in July, including a $100 million AbbVie milestone, and reaffirmed 2026-2027 timelines for RGX-202, sura-vec and RGX-121.
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The company filed an amendment lifting its at-the-market offering capacity by $500 million after selling $550 million in shares under the original agreement.
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Lyell says its PiNACLE trial in LBCL remains on track and reports the amendment of its LYL273 mCRC study to a Phase 1/2 design after new safety data.
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Two Phase 1 studies continue enrolling and cash of $190.0 million is expected to fund operations into 2H 2028, the company said.
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The company said the oversubscribed PIPE deal drew existing Alkeus Pharmaceuticals investors after Tarsus announced its planned acquisition of Alkeus.
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The company also discontinued EVO756 development in chronic spontaneous urticaria and pointed to cash lasting through 2028.
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The company posted 34% year-over-year growth in net product revenue, driven by Recorlev, and narrowed its 2026 revenue outlook to $385 million to $390 million.
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Sionna Therapeutics says its Phase 2a trial of SION-719 and its Phase 1 dual-combination trial with SION-451 both remain on schedule to deliver topline data this summer.
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Tarsus reported $173.9 million in second quarter XDEMVY sales and disclosed a pending acquisition of Alkeus Pharmaceuticals along with a $125 million private placement.
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BioLife reported 21% revenue growth and a GAAP net income boosted by a tax benefit while confirming its pending sale to Repligen is expected to close in the fourth quarter of 2026.
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Trevi Therapeutics reported second-quarter 2026 results, with cash and securities of $318.9 million and a cash runway extended into 2030.
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The company reiterated its full-year revenue and expense guidance while highlighting new real-world and Phase 2 myelofibrosis data and progress on its Phase 3 IMpactMF trial.
SEC filing