-
Curis shareholders approve reverse stock split authorization up to 1-for-25
26.9M votes for, 752K against, 124K abstain on reverse split proposal.
-
Curis stockholders approve doubling of authorized common shares to 567.5M
Authorized common shares increased to 567,514,300 from 283,757,150; total capital stock to 572,514,300.
-
Curis Q1 net loss $24.2M, no revenue; cash $15M; clinical milestones ahead
Net loss of $24.2M ($1.25 per share) vs $10.6M loss in Q1 2025; EPS unchanged due to higher share count.
-
Curis receives Nasdaq delisting notice due to bid price below $1.00 for 30 days
Received Delist Determination Letter from Nasdaq on April 27, 2026.
-
Curis Q4 net income $19.4M on Erivedge gain; PIPE raises $20.2M initial
FY2025 net loss $7.6M ($0.58/shr) vs $43.4M ($6.88/shr) in FY2024; Q4 net income $19.4M ($1.23/shr).
-
Curis shareholders approve authorized share increase from 73.3M to 288.8M and 2026 Incentive Plan
Authorized common stock increased from 68.3M to 283.8M; total capital stock from 73.3M to 288.8M, effective March 17, 2026.
-
Curis regains Nasdaq compliance but faces one-year discretionary monitor
Received Nasdaq notice on Feb 3, 2026 that it regained compliance with MVLS Rule (Rule 5550(b)(2)).
-
Curis raises up to $80.8M in PIPE financing; extends cash runway into 2027
Initial gross proceeds of ~$20.2M from sale of Series B Preferred Stock and warrants; potential total up to ~$80.8M if warrants exercised.
-
Curis sells Erivedge royalty interest for $2.5M; pro forma shows $28M gain
Sold Curis Royalty LLC to Oberland Capital for $2.5M upfront plus release of $28.6M liability.
-
Curis sells Erivedge royalty rights to Oberland for $2.5M; Q3 net loss narrows to $7.7M
Sold Erivedge IP and license rights to Oberland affiliate for $2.5M upfront and release of future royalty liability.
-
Nasdaq grants Curis exception until Nov 14, 2025 to meet $35M MVLS rule
Company received Nasdaq delisting notice on Aug 21, 2025 for failing $35M market value requirement.
-
Curis receives Nasdaq delisting notice for market value below $35M; plans appeal
On Aug 21, 2025, Curis received Nasdaq delisting notice for failing MVLS Requirement (market value <$35M for 30 consecutive days).
-
Curis files prospectus supplement for up to $8.14M common stock ATM offering
Up to $8,137,047 in common stock offered via ATM under existing Sales Agreement with Cantor Fitzgerald & JonesTrading.
-
Curis Q2 2025 net loss $8.6M; cash runway extended to Q1 2026 via $6M offering
Net loss $8.6M ($0.68/sh) vs $11.8M ($2.03/sh) in Q2 2024; revenue $2.7M from Erivedge royalties.
-
Curis raises $7.0M in registered direct & private placement; cash runway into Q1 2026
Gross proceeds ~$7.0M from sale of 1,538,460 shares and warrants; combined price $2.275/share + warrant.
-
Curis shareholders approve doubling of authorized common shares, quorum reduction, and equity plan increase
Authorized common shares increased from 34.2M to 68.3M; total capital stock from 39.2M to 73.3M.
-
Curis Q1 net loss $10.6M, appoints Dr. Hamdy CMO, emavusertib progress
Net loss $10.6M ($1.25/share); cash $20.3M; runway into Q4 2025.
-
Curis gains FDA & EMA support for accelerated approval of emavusertib in PCNSL
FDA and EMA agree TakeAim Lymphoma study may support accelerated approval path for PCNSL.
-
Curis raises ~$10M; FY2024 net loss $43.4M; FDA/EMA see path for PCNSL drug
Gross proceeds ~$10M from sale of 1.97M shares and pre-funded warrants for 2.18M shares, plus common warrants for 8.32M shares at $2.41.
-
Curis receives Nasdaq notice of non-compliance with market value listing requirement
Market value of listed securities below $35M for 30 consecutive business days as of Feb 21, 2025.
-
Curis Q3 net loss narrows to $10.1M; emavusertib shows durable responses in BTKi-progressed PCNSL
Net loss of $10.1M ($1.70 per share) vs $12.2M ($2.13) in Q3 2023; nine-month net loss $33.8M.
-
Curis raises $12.1M via registered direct offering and concurrent private placement
Issued 2,398,414 shares of common stock and unregistered warrants for 2,398,414 shares at exercise price $4.92.
-
Curis Q2 net loss $11.8M; emavusertib gets EU ODD for PCNSL
Net loss of $11.8M ($2.03/sh) vs $12.0M ($2.47) in Q2 2023; revenue $2.5M from Erivedge royalties.
-
Curis cuts workforce ~30%, focuses on combo studies; cash runway into 2025
Board approved ~30% workforce reduction as monotherapy trials near completion.
-
Curis expands TakeAim Leukemia study to 30 patients; 6/11 FLT3m and 4/18 SFm respond
TakeAim Leukemia dataset expanded from 5 to 30 R/R AML patients (25 new) with emavusertib monotherapy at 300 mg BID.
-
Curis Q1 net loss $11.9M ($2.05/sh); cash $40.7M; topline AML data May 14
Net loss $11.9M vs $11.6M Q1 2023; revenue $2.1M (Erivedge royalties) vs $2.3M.
-
Curis Q4 2023 net loss $11.7M ($2.03/sh); cash $56.3M, clinical data from ASH shows CRs
Net loss for Q4 2023 was $11.7M ($2.03/share) vs $11.3M ($2.35/share) in Q4 2022.
-
Curis files updated corporate slide presentation; no material new details evident
Company furnished a corporate slide presentation under Item 7.01, dated January 2024.
-
Curis Q3 net loss $12.2M ($2.13/sh); cash $68.5M; emavusertib studies resume
Net loss narrowed to $12.2M from $13.3M YoY; revenue unchanged at $2.8M from Erivedge royalties.
-
Curis stockholders approve 1-for-20 reverse stock split and increase in authorized shares
Stockholders approved increase in authorized common shares from 227,812,500 to 455,625,000 at Special Meeting on Sept 26.
-
Curis approves 1-for-20 reverse stock split; authorized common shares set at 22.78M after amendments
Special meeting on Sept 26, 2023 approved 1-for-20 reverse stock split; effective Sept 28, trading on split-adjusted basis Sept 29.
-
Curis Q2 net loss $12.0M ($0.12/sh); FDA lifts partial clinical hold on TakeAim Leukemia study
Net loss $12.0M ($0.12/sh) vs $15.9M ($0.17/sh) in Q2 2022; six-month net loss $23.5M ($0.24/sh).
-
FDA lifts partial clinical hold on Curis leukemia study; RP2D set at 300 mg BID
FDA removed partial clinical hold on TakeAim Leukemia Phase 1/2 study of emavusertib (CA-4948).
-
Curis prices $15.1M registered direct offering of 18.4M shares at $0.82/share
Offering led by existing investors; 18.4M shares sold at $0.82 per share.
-
Curis shareholders elect directors, approve say-on-pay, and ratify auditor at 2023 annual meeting
Martyn D. Greenacre and Kenneth I. Kaitin elected as Class III directors with 30.4M and 26.8M votes for, respectively.
-
Curis Q1 net loss narrows to $11.6M; enrolls 9 patients for emavusertib; new CDO
Net loss $11.6M ($0.12/share) vs $16.1M ($0.18) YoY; revenue $2.3M, up from $2.1M.
-
Curis receives Nasdaq approval to transfer to Capital Market; extended bid-price compliance deadline to Oct 16, 2023
Transfer from Nasdaq Global Market to Nasdaq Capital Market effective April 24, 2023.
-
Curis completes FDA-requested enrollment for emavusertib; FY2022 net loss $56.7M
Completed enrollment of 9 additional patients at 200mg BID for TakeAim Leukemia study ahead of schedule; expects data in Q2, FDA meeting in Q3 for partial clinical hold resolution.
-
Curis Q3 net loss $13.3M, cuts ~30% of workforce to focus on emavusertib, cash runway into 2025
Net loss of $13.3M ($0.14/shr) vs $11.1M ($0.12/shr) in Q3 2021; revenues $2.8M.
-
Curis receives Nasdaq deficiency notice for bid price below $1.00; 180-day cure period
On Oct 21, 2022, Nasdaq notified Curis its common stock bid price closed below $1.00 for 30 consecutive business days, violating Listing Rule 5450(a)(1).
-
Curis elects Anne E. Borgman, M.D. to board of directors
Anne E. Borgman, M.D. elected as Class I director effective Oct 12, 2022, term until 2024 annual meeting.
-
Director Lori Kunkel resigns from Curis board citing fundamental disagreement on operations
Resignation effective September 30, 2022; she served on Nominating/Corporate Governance and chaired Clinical Program Committee.
-
FDA allows Curis to resume enrollment in Phase 1a of emavusertib leukemia study
FDA removed partial clinical hold on monotherapy dose-finding (Phase 1a) of TakeAim Leukemia study after reviewing rhabdomyolysis data.
-
FDA lifts partial clinical hold on Curis's TakeAim Lymphoma study of emavusertib
FDA lifted partial clinical hold on TakeAim Lymphoma Phase 1/2 study; enrollment to resume Q3 2022.
-
Curis Q2 net loss widens to $15.9M; appoints new CFO; emavusertib combo shows tumor reduction in 8 of 9
Net loss of $15.9M ($0.17/sh) vs $10.8M ($0.12) in Q2 2021; revenue flat at $2.4M.
-
Curis CFO William Steinkrauss resigns effective Aug 5, 2022; consulting transition
William Steinkrauss notified Curis of resignation on June 27, 2022 to pursue entrepreneurial opportunity.
-
Curis shareholders elect Hohneker but substantial withhold votes for director Rubin at 2022 annual meeting
John A. Hohneker re-elected with 42,274,804 for vs 3,584,620 withheld (23M broker non-votes).
-
Curis Q1 net loss $16.1M; cash $120.7M; emavusertib studies on partial clinical hold
Net loss $16.1M ($0.18/sh) vs $9.9M in Q1 2021; revenue $2.1M unchanged.
-
FDA partial clinical hold on Curis' TakeAim Lymphoma study; no new enrollment
FDA placed partial clinical hold on Phase 1/2 TakeAim Lymphoma study of emavusertib in B-cell malignancies.
-
FDA partial clinical hold on Curis leukemia study after patient death; lymphoma study paused
FDA partial clinical hold on TakeAim Leukemia Phase 1/2a (NCT04278768); no new patients enrolled.