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Chiesi completes $27/share acquisition of KalVista; shares cease trading on Nasdaq
Tender offer accepted 43,152,532 shares (~77.8% of outstanding) at $27.00 cash per share.
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Chiesi Group to acquire KalVista Pharmaceuticals for $27.00 per share, ~$1.9bn
Chiesi will acquire all KalVista shares for $27.00/sh cash, a 36% premium to 30-day VWAP as of April 28, 2026.
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KalVista reports $49.1M EKTERLY revenue in 8mo transition period, 1,702 patient start forms
Global net product revenue of $49.1M from EKTERLY (sebetralstat) for May–Dec 2025; first commercial sales since launch on July 7, 2025.
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KalVista reports preliminary Q4 EKTERLY revenue of ~$35M, full-year ~$49M; 1,318 patient start forms
Preliminary unaudited global net product revenue: ~$35M for Q4 2025, ~$49M for full year 2025.
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KalVista reports $13.7M Q3 net product revenue from EKTERLY launch; 937 patient start forms through Oct
Net product revenue of $13.7M for Q3 ended Sept 30, 2025, first full quarter of EKTERLY commercial launch.
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KalVista appoints Bilal Arif as COO and Linea Aspesi as Chief People Officer
Bilal Arif appointed COO effective Oct 6, 2025; base salary $520k, annual bonus target 40%, option grant of 100,000 shares.
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KalVista appoints Bethany Sensenig to Board and Audit Committee; annual meeting results filed
Bethany Sensenig appointed to Board and Audit Committee effective October 1, 2025.
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KalVista closes $143.75M convertible notes offering; net proceeds ~$139M for EKTERLY
Issued $143.75M in 3.250% Convertible Senior Notes due 2031, including full exercise of $18.75M greenshoe.
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KalVista Q1: EKTERLY approved in US/UK; 460 patient start forms; positive CHMP opinion
EKTERLY (sebetralstat) FDA approved July 7, 2025; UK MHRA authorized same month; positive CHMP opinion; EU decision expected Oct 2025.
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KalVista sets June 18, 2026 as annual meeting date; stockholder deadlines revised
2026 Annual Meeting set for June 18, 2026; changed >30 days from 2025 meeting.
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KalVista FY2025: FDA approved EKTERLY; cash $220.6M; R&D down, G&A up
FDA approved EKTERLY (sebetralstat) on July 7, 2025 as first oral on-demand HAE treatment; U.S. launch underway.
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KalVista receives FDA approval for EKTERLY (sebetralstat), first oral on-demand HAE treatment
FDA approved EKTERLY for acute attacks of hereditary angioedema in patients 12+ years; first oral on-demand therapy.
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KalVista COO Jebediah T. Ledell resigns effective May 12, 2025
COO Jebediah T. Ledell resigned effective immediately on May 12, 2025.
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KalVista licenses sebetralstat Japan rights to Kaken; $11M upfront, up to $24M total plus royalties
Upfront payment of $11M plus up to $11M regulatory milestone expected in early 2026.
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KalVista changes fiscal year-end from April 30 to December 31
Board approved change effective March 13, 2025; new fiscal year begins January 1, 2026.
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KalVista Q3 fiscal 2025: $253.2M cash, sebetralstat regulatory progress; PDUFA June 17
No revenue; R&D expense $12.6M (down from $22.5M YoY); G&A $30.3M (up from $10.6M) due to pre-commercial activities.
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KalVista appoints Jeb Ledell as COO; base salary $500k, 100k stock options
Jebediah T. Ledell appointed COO effective December 16, 2024; brings 20+ years biotech ops experience.
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KalVista Q2 FY2025: No revenue, cash $135.8M; sebetralstat NDA accepted with PDUFA June 17, 2025
R&D expenses $16.6M, G&A $29.2M; pro forma cash $292.2M after $156.4M net November raise.
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KalVista appoints Laurence Reid, Ph.D. to Board of Directors
Laurence Reid appointed to KalVista Board effective Nov 23, 2024; term expires at 2027 annual meeting.
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KalVista secures up to $179M synthetic royalty financing with DRI for sebetralstat launch
Upfront payment of $100M; potential total up to $179M including $22M optional approval payment and $57M sales milestone.
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KalVista raises $60M in public offering and private placement to fund sebetralstat
Public offering of 5.5M shares at $10.00 per share for gross proceeds of $55M; net ~$51.3M.
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KalVista shareholders elect directors, ratify auditor, approve say-on-pay at 2024 annual meeting
William Fairey and Nancy Stuart elected as Class III directors with 30.2M and 19.3M votes 'For', respectively; Stuart faced 11.7M votes 'Against'.
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KalVista appoints Brian Piekos as CFO effective Sept 9; 100K stock option inducement granted
Brian Piekos joins as CFO; previously CFO of Elicio Therapeutics and Gemini Therapeutics.
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KalVista Q1 net loss $40.4M; FDA accepts NDA for sebetralstat, PDUFA June 17, 2025
Net loss $40.4M ($0.87/share) vs $25.3M prior year; no revenue recognized.
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KalVista Pharmaceuticals enters lease for HQ and lab in Framingham; aggregate rent ~$11.2M
Lease for 32,110 sq ft at 200 Crossing Blvd, Framingham, MA, as corporate HQ and lab space.
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KalVista submits NDA for sebetralstat; FY2024 net loss $126.6M
NDA submitted to FDA for sebetralstat, first oral on-demand HAE treatment; potential approval H1 2025.
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KalVista appoints William Fairey to Board; commercial expertise in rare disease
William Fairey appointed to Board effective April 18, 2024 as Class III director.
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KalVista reports Phase 3 KONFIDENT success for sebetralstat, CEO transition, $150M financing
Phase 3 KONFIDENT met all primary and key secondary endpoints; sebetralstat safety profile similar to placebo.
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KalVista appoints Benjamin Palleiko as CEO; Crockett resigns in planned transition
T. Andrew Crockett resigned as CEO and board director effective March 6, 2024, not due to any disagreement.
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KalVista prices $160.1M public offering of common stock and pre-funded warrants
Offering includes 7,016,312 shares at $15.25 and pre-funded warrants for 3,483,688 shares; gross proceeds $160.1M.
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KalVista terminates $100M ATM sales agreement with Cantor Fitzgerald; no shares sold
Terminated Controlled Equity Offering Sales Agreement with Cantor, effective Feb 14, 2024.
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KalVista announces positive Phase 3 KONFIDENT results; sebetralstat meets all endpoints with rapid symptom relief
Sebetralstat 300 mg achieved beginning of symptom relief in median 1.61 hours vs placebo 6.72 hours (p<0.0001).
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KalVista hits Phase 3 attack target for sebetralstat; NDA on track for H1 2024
Phase 3 KONFIDENT trial achieved targeted number of attacks; data readout early 2024, NDA filing expected H1 2024.
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KalVista stockholders approve officer exculpation amendment, elect directors
Approved certificate of amendment to limit officer liability under Delaware law (20.2M for, 2.5M against).
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KalVista reports Q1 FY2024 net loss $25.3M; KONFIDENT phase 3 enrollment achieved
Net loss $25.3M ($0.74/share) vs $23.0M ($0.94/share) in prior-year quarter.
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KalVista FY2023 net loss $92.9M; sebetralstat Phase 3 enrollment complete
Phase 3 KONFIDENT trial achieved target enrollment (114 patients); data readout expected Q4 2023; NDA planned H1 2024.
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KalVista amends CFO employment agreement raising base salary to $565K; updates bylaws for universal proxy rules
CFO Benjamin L. Palleiko's base salary raised to $565,000 (effective May 1, 2023); target bonus increased to 50% of salary.
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KalVista reports Q3 net loss $21.3M; sebetralstat phase 3 enrollment >50%, data H2 2023
Net loss $21.3M ($0.75 per share), no revenue; R&D $20.1M, G&A $6.9M.
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KalVista promotes CFO/CBO Palleiko to President; cites $190M cash for sebetralstat launch prep
Benjamin L. Palleiko appointed President effective Jan 4, 2023, while retaining CFO and CBO roles.
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KalVista raises ~$58M in registered direct offering of 9.48M shares at $6.00/share plus warrants
9,484,199 shares at $6.00 per share, plus pre-funded warrants for 182,470 shares at $5.999 each.
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KalVista terminates KVD824 Phase 2 trial over liver enzyme elevations; net loss widens to $22.3M
Phase 2 KOMPLETE trial for KVD824 terminated due to patient liver enzyme elevations; future development uncertain.
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KalVista Pharmaceuticals appoints Brian J.G. Pereira as Chairman; Martin Edwards resigns in planned transition
Martin Edwards resigned as Chairman and director effective immediately; departure not due to any disagreement.
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KalVista Q1 net loss $23.0M ($0.94/share); cash $142.1M, down $24.1M from April
No revenue; R&D spending rose to $18.2M (vs. $13.7M a year ago), driven by Phase 3 KONFIDENT and preclinical costs.
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KalVista FY2022 net loss $82.3M (-$3.36/share); cash $166.2M; sebetralstat Phase 3 on track
Net loss $82.3M ($3.36 loss per share) vs $46.2M ($2.42) prior year; R&D spend $70.2M.
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KalVista director Daniel Soland resigns; Patrick Treanor appointed to board
Daniel Soland resigned from board and committees effective May 25, 2022; not due to any disagreement with the Company.
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KalVista reports Q3 net loss $22.5M; KVD900 Phase 3 trial initiated, data expected H2 2023
Net loss of $22.5M ($0.92/share) vs $10.0M loss ($0.56) YoY; R&D spend $19.7M (up from $9.1M).
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KalVista initiates Phase 3 KONFIDENT trial of KVD900 for HAE attacks
KVD900 is first potential oral on-demand therapy for HAE; all current on-demand therapies are injectable.
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KalVista reports Q2 net loss $19.7M; advances HAE oral candidates KVD900 and KVD824
Net loss of $19.7M ($0.80 per share) for quarter ended Oct 31, 2021 vs $10.4M ($0.58) year ago.
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KalVista stockholders elect three Class III directors at 2021 annual meeting
Elected Albert Cha, Martin Edwards, and Nancy Stuart as Class III directors for three-year terms expiring 2024.
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FDA lifts clinical hold on KalVista's Phase 2 KVD824 trial for HAE prophylaxis
FDA removed clinical hold on Phase 2 KOMPLETE trial of KVD824 for oral prophylactic treatment of hereditary angioedema.