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Lisata Therapeutics cuts 72% of workforce, sues Kuva Labs over merger breach
Workforce reduced by ~72% effective immediately; estimated $1.2M in severance costs through Q3 2026.
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Lisata Therapeutics terminates merger with Kuva Labs; Kuva failed to secure financing
Merger agreement terminated after Kuva Labs failed to obtain financing to fund tender offer.
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Kuva Labs delays tender offer for Lisata to June 10; outside date extended to July 17
Tender offer commencement deadline extended from June 1 to June 10, 2026; company waives claims for previous delay.
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Kuva Labs notifies Lisata it will not commence tender offer on June 1 as agreed; deal uncertain
On May 31, Kuva Labs told Lisata it will not start the tender offer on June 1 as previously agreed and amended.
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Lisata amends merger: cash per share cut from $5 to $4, CVR increased to up to $3
Cash consideration reduced from $5.00 to $4.00 per share; CVR now offers up to $3.00 total ($1.25 + $1.75 milestone payments).
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Lisata extends tender offer deadline to May 29; Kuva to pay up to $1.1M in expenses
Tender offer commencement extended from April 13 to May 29, 2026, under amended merger agreement.
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Lisata acquisition in limbo: Kuva Labs delays tender offer, seeks new financing
Kuva Labs has not yet commenced tender offer for Lisata; deadline extended from April 3 to April 13, 2026.
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Lisata to be acquired by Kuva Labs for $5.00 per share plus contingent $1.00 CVR
Kuva Labs will acquire all Lisata common shares for $5.00 cash plus one non-tradeable CVR potentially paying $1.00 upon FDA filing for certepetide.
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Lisata Therapeutics terminates exclusive license for certepetide with Qilu Pharmaceutical
Mutual termination of 2021 License and Collaboration Agreement with Qilu, effective January 23, 2026.
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Lisata to be acquired by Kuva Labs for $4.00 cash/share + up to $2 CVRs; ~85% premium
All-cash tender offer at $4.00/share plus two non-tradeable CVRs worth up to $2/share tied to certepetide milestones.
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Lisata reports Q3 2025 net loss $4.2M; cash runway into Q1 2027 with new partnerships
Net loss $4.2M vs $4.9M in Q3 2024; operating expenses down 17% to $4.4M.
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Lisata grants Catalent non-exclusive license for certepetide ADC payload; up to $10.5M milestones
Granted Catalent non-exclusive license to use certepetide as ADC payload in SMARTag platform; Catalent assumes all R&D/commercial costs.
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Lisata Therapeutics granted US composition-of-matter patent for certepetide expiring 2040
U.S. Patent No. 12,351,653 covers certepetide's chemical structure and pharmacokinetic properties.
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Positive Cohort B ASCEND data: 6M PFS 60.8% (certepetide) vs 25% (placebo)
Cohort B: median PFS 7.5 months (certepetide) vs 4.7 months (placebo); ORR 45.2% vs 19%.
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Lisata Q1 net loss $4.7M; cash $25.8M; ASCEND Cohort B oral at ESMO-GI Jul 2025
Net loss $4.7M for Q1 2025, vs $5.4M in Q1 2024; operating expenses down 11% to $5.8M.
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Lisata Therapeutics reports 2024 net loss $20M, cash $31.2M; promising Phase 2b pancreatic cancer data
Revenue $1.0M from Kuva license (vs $0 in 2023); operating expenses down 8.9% to $23.4M.
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Lisata reports Phase 2 ASCEND Cohort A: mOS 12.68 vs 9.72 months; 4 complete responses
Cohort A: median OS of 12.68 months for certepetide plus chemo vs 9.72 months for placebo plus chemo.
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Lisata Therapeutics Q2 2024 net loss $5.0M; ASCEND Phase 2b top-line data expected Q4 2024
Net loss $5.0M in Q2 2024 vs $4.0M in Q2 2023; operating expenses down 19.7% to $5.5M.
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Lisata Q1 net loss $5.4M; ASCEND Phase 2b data on track for Q4 2024
Cash, equivalents and marketable securities $43.3M as of Mar 31, 2024; funding operations into early 2026.
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Lisata Q3 net loss $5.3M; ASCEND ~95% enrolled, BOLSTER first patients treated
Net loss of $5.3M in Q3 2023 (vs $37.4M prior year which included $30.4M merger costs); cash $54.4M.
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Lisata Q2 net loss $4.0M, extends cash runway to Q1 2026; tech transfer deal for TPN platform
Net loss $4.0M in Q2 2023 vs $6.6M in Q2 2022, down 40% due to $2.2M NJ tax credit.
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Lisata Therapeutics reports FY2022 financial results and provides business update
Net loss for FY2022 was $54.2 million, including $30.4 million non-routine merger-related IPR&D expense.
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Lisata's LSTA201 trial in diabetic kidney disease fails to show consistent kidney function improvement
Preliminary unaudited cash, equivalents and marketable securities of ~$69.2M as of Dec 31, 2022.
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Lisata Therapeutics Q3 net loss widens to $37.4M on merger costs; cash $75.5M; LSTA1 trials on track
Net loss $37.4M (Q3 2022) vs $6.9M (Q3 2021), driven by merger-related expenses and stock compensation.
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Lisata halts XOWNA FREEDOM Trial; development now contingent on partner
Phase 2b FREEDOM Trial of XOWNA (autologous CD34+ cells) suspended May 2022 due to COVID enrollment challenges and heterogeneity.
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Lisata Therapeutics formed via Caladrius-Cend merger; ~$76M cash, ticker LSTA
Merger closed 9/15/22: Caladrius issued 0.5338 shares per Cend share after 1:15 reverse split; post-merger shares ~7.82M.
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Caladrius stockholders approve merger with Cend Therapeutics, 1:15 reverse split, name change to Lisata Therapeutics
Merger with Cend approved: 25,973,235 for, 2,912,622 against, 172,676 abstain.
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Caladrius receives Nasdaq extension to Feb 13, 2023 to regain $1 bid price compliance
Company failed to meet $1 minimum bid price by Aug 17, 2022 initial compliance deadline.
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Caladrius Q2 net loss $6.6M; merger with Cend on track for Q3 2022 forming Lisata Therapeutics
Net loss $6.6M vs $5.7M YoY; cash $73M after $10M Cend investment.
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Caladrius suspends enrollment in Phase 2b FREEDOM Trial of XOWNA; interim analysis expected Aug 2022
Enrollment paused in 105-patient double-blind placebo-controlled FREEDOM Trial; only ~35 patients enrolled to date.