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Climb Bio Announces Positive Initial Phase 1b Data for Budoprutug in Immune Thrombocytopenia
Phase 1b enrolled 15 patients at 250 mg (n=6) and 500 mg (n=9) doses, median follow-up 38 and 12 weeks respectively.
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Climb Bio reports positive Phase 1 safety data for CLYM116; plans Phase 2 in IgAN in Q3 2026
Translational PK/PD model from NHP data projects dose-dependent IgA suppression, suggesting less-frequent dosing.
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Climb Bio reports Q1 2026 cash of $146.3M; $110M private placement closed April 29
R&D expense $9.4M vs $17.3M YoY (incl. $9M CLYM116 upfront in prior year); G&A $5.8M.
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Climb Bio reports positive SC formulation data; ITP data June 2026, pMN/SLE Q4 2026
Topline Phase 1 SC data: robust B-cell depletion similar to IV; generally safe and well-tolerated.
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Climb Bio raises $110M in private placement of common stock and pre-funded warrants
Gross proceeds of ~$110M from 9.481M shares at $9.50 and 2.106M pre-funded warrants at $9.4999 each.
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Climb Bio reports Q4/FY2025 results; cash $160.7M; pipeline trials on track with data in 2026
Cash, cash equivalents, and marketable securities $160.7M as of Dec 31, 2025; expected runway into 2028.
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Climb Bio updates on budoprutug and CLYM116 trials; cash runway into 2028
First patient dosed in PrisMN Phase 2 trial of budoprutug for primary membranous nephropathy (Nov 2025).
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Climb Bio sues Alumis to avoid $3M milestone payment, disputes 'Product' definition under APA
Filed complaint in Delaware Superior Court seeking declaratory judgment that budoprutug is not a 'Product' under the APA.
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Climb Bio exchanges 20.44M shares for pre-funded warrants; RA Capital voting capped at 33%
Exchanged 20,440,000 shares for pre-funded warrants with $0.0001 exercise price via Section 3(a)(9) exemption.
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Climb Bio Q3 2025 cash $175.8M; pipeline advances with budoprutug and CLYM116 trials
Cash and equivalents $175.8M as of Sep 30, 2025; runway expected through 2027.
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Climb Bio reports long-term Phase 1b data for budoprutug; up to 3-year proteinuria control
Abstract published for budoprutug (anti-CD19 mAb) showing durable proteinuria control up to 3 years in four PMN patients.
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Climb Bio appoints Susan Altschuller as CFO, grants 600,000 stock options
Appointed Susan Altschuller, Ph.D., MBA, as CFO and Treasurer effective Oct 1, 2025; previously CFO at Cerevel and ImmunoGen.
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Climb Bio reports CLYM116 preclinical data showing >70% IgA reduction and longer half-life vs sibeprenlimab
In nonhuman primate study, CLYM116 showed ~2-3 times longer half-life and deeper IgA reduction vs sibeprenlimab at 6 mg/kg.
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Climb Bio Q2 cash $187.4M, R&D $6.6M; budoprutug trials underway; new CMO
Cash and marketable securities $187.4M as of June 30, 2025; cash runway expected through 2027.
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COO Brett Kaplan departs Climb Bio; CEO Aoife Brennan named interim PFO
Brett Kaplan, COO and principal financial officer, separated mutually on May 23, 2025.
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Climb Bio reports Q4/FY2024 results, cash $212.5M through 2027; launches $22.35M ATM offering
Entered ATM equity offering of up to $22.35M via Oppenheimer; 3% commission; proceeds to support pipeline.
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Climb Bio licenses MIL116 antibodies from Mabworks; reports $212.9M cash, runway through 2027
Upfront $9M to Mabworks; up to $30M development/regulatory milestones for first indication.
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Climb Bio Q3 net loss $8.9M; cash $217.9M through 2027; FDA IND cleared for SLE trial
Net loss $8.9M for Q3 2024 vs $4.0M Q3 2023; R&D expenses $6.2M, G&A $5.5M.
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Climb Bio outlines budoprutug development strategy; Phase 1b pMN data shows 60% remission
Approximately $218M cash at Sept 30, 2024; expected to fund operations through 2027.
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Eliem Therapeutics CSO departs, CFO role changed, Executive Chairman resigns amid strategic pivot
Valerie Morisset, EVP R&D and CSO, separated August 23; settlement provides 18 months base salary, pro rata bonus, accelerated equity vesting.
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Eliem Therapeutics Q2 net loss $54.9M; completed Tenet Medicines acquisition and $120M financing
Completed acquisition of Tenet Medicines and concurrent $120M private placement in June 2024.
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Eliem closes acquisition of Tenet Medicines, gains TNT119 autoimmune drug, raises $120M PIPE
Acquisition of Tenet closed June 27; 5,560,047 Eliem shares issued to Tenet equityholders.
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Shareholders approve Eliem-Tenet merger; closing expected June 27, 2024
Share Issuance Proposal passed: 26,311,239 for, 3,253 against; disinterested approval 12,655,083 for.
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Eliem to acquire Tenet Medicines in stock deal; raises $120M PIPE at $3.84/share
Eliem (ELYM) acquires Tenet via merger; Tenet holders get 15.4% of combined co. stock.
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Eliem receives non-binding term sheet to acquire biotech Tango for $20M in stock
RA Capital owns ~47.5% of Eliem and majority of Tango; special committee oversees strategic review.
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Eliem halts Kv7 program, explores strategic alternatives including sale or merger
Halts further development of Kv7 program; shifts focus to maximizing shareholder value.
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Eliem Therapeutics Announces CFO Resignation and Appoints New Principal Financial and Accounting Officers
Erin Lavelle resigned as EVP, COO, and CFO effective March 10, 2023.
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Eliem restructures, pauses ETX-155, focuses on Kv7 program, extends cash runway into 2027
Corporate reorganization: pause ETX-155 (GABA A PAM) development, focus on Kv7 program lead ETX-123; workforce reduction ~55% in H1 2023.
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Eliem Therapeutics pauses ETX-155, cuts workforce 55%, CEO and CFO depart; cash $123.6M
Pauses development of ETX-155 (Phase 2-ready for MDD) to focus on preclinical Kv7.2/3 program (ETX-123).
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Eliem Therapeutics Q3 net loss $9.7M, cash $129.6M; ETX-155 Phase 2a MDD trial to start Q1 2023
Net loss of $9.7M for Q3 2022 (vs. $9.6M Q3 2021); R&D expenses $4.3M, G&A $4.5M.
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Eliem Therapeutics ETX-155 update; Phase 2a MDD on track for Q1 2023; cash $129.8M
Cash, cash equivalents and investments of $129.8M as of Sept 30, 2022 (includes $6.2M tax reimbursements); funds operations into 2025.
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Eliem Therapeutics Q2 net loss $14.6M; discontinues ETX-810 Phase 2a after failure
Net loss of $14.6M for Q2 2022 vs $8.7M in Q2 2021; cash, equivalents, securities $134.7M.
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Eliem delays ETX-155 Phase 2a MDD trial to Q1 2023 after lower exposure in PSE trial; CMC issue identified
Lower-than-expected ETX-155 exposure in Phase 1b photosensitive epilepsy trial attributed to CMC batch inconsistencies.
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Eliem Q1 net loss $13.2M; ETX-810 fails DPNP trial; ETX-155 data inconclusive; LSRP data Q3
Net loss of $13.2M in Q1 2022 vs $18.6M in Q1 2021; cash $149.9M, funded through at least 2023.