-
Atossa Q2 2026: OpEx $8.7M, R&D $4.9M; raises up to $16.5M from offering
Total operating expenses $8.7M in Q2 2026, down $0.3M from $9.0M in Q2 2025.
-
Atossa raises $4.5M in registered direct offering of stock and warrants
Sold 1,363,638 shares at $3.30/share plus Series A and B warrants for 1,363,638 shares each at $4.40.
-
Atossa shareholders approve reverse stock split up to 20:1, re-elect directors
Reverse stock split amendment approved: 2,336,815 for, 1,866,873 against, 33,271 abstentions.
-
Operating expenses $9.9M, up 34% YoY; FDA grants RPD for (Z)-endoxifen in DMD and McCune-Albright
Total operating expenses $9.9M in Q1 2026, up from $7.4M in Q1 2025, driven by higher legal fees for patent litigation (subsequently settled) and R&D costs.
-
Atossa settles patent disputes with Intas; Endoxifen patents remain enforceable
Entered Settlement Agreement on April 13, 2026 with Intas Pharmaceuticals and Jina Pharmaceuticals to resolve Endoxifen patent disputes.
-
Atossa Therapeutics Reports Q4 and FY2025 Results, Highlights (Z)-Endoxifen Progress in DMD
Atossa reported FY2025 operating expenses of $37.1M, up from $27.6M; R&D expenses increased 50% to $21.2M.
-
Atossa enters $50M ATM equity offering with Rodman & Renshaw; terminates Jefferies facility
ATM agreement allows up to $50M in common stock sales; company pays 3% commission to sales agent.
-
Atossa Therapeutics regains Nasdaq compliance on minimum bid price requirement
Received Nasdaq letter on Feb 17, 2026 confirming compliance with Listing Rule 5550(a)(2).
-
Atossa receives FDA Rare Pediatric and Orphan Drug designations for (Z)-endoxifen in DMD; pauses MBC
FDA Rare Pediatric Disease and Orphan Drug designations granted for (Z)-endoxifen in Duchenne Muscular Dystrophy (Dec 2025/Jan 2026).
-
Atossa shareholders approve 15:1 reverse stock split effective Feb 2, 2026
Approved at Special Meeting: 33.7M for, 27.9M against, 0.1M abstentions; no broker non-votes.
-
Atossa reports preliminary cash balance of ~$40M, limited other details
Estimated cash and cash equivalents of ~$40M as of Dec 31, 2025, preliminary and unaudited.
-
Atossa Therapeutics receives FDA 'Study May Proceed' letter for (Z)-Endoxifen metastatic breast cancer trial
FDA issued 'Study May Proceed' letter for Atossa's IND for (Z)-Endoxifen in metastatic ER+/HER2- breast cancer.
-
Atossa completes FDA Type C meeting; gains clarity on accelerated (Z)-endoxifen development
FDA provided feedback on regulatory pathways for (Z)-endoxifen across metastatic, neoadjuvant, and risk-reduction settings.
-
Atossa advances (Z)-endoxifen regulatory path; Q3 op-ex $9.3M
FDA Type C meeting set Nov 17 to discuss accelerated NDA path for (Z)-endoxifen in breast cancer risk reduction; written comments received.
-
Atossa appoints Mark Daniel as CFO to lead finance for commercial readiness
Mark Daniel appointed CFO effective Oct 14; Heather Rees transitions to non-officer employee through Nov 15.
-
Atossa Therapeutics posts updated corporate presentation; no specific financial details provided
Filed as Exhibit 99.1 on September 26, 2025, but presentation content not included in this filing text.
-
Atossa requests FDA Type C meeting to accelerate low-dose (Z)-endoxifen for breast cancer risk reduction
Company requested a Type C FDA meeting; expects update by year-end 2025.
-
Atossa Therapeutics receives Nasdaq extension to Feb 17, 2026 for bid price compliance
Nasdaq notified Atossa on Feb 21, 2025 of non-compliance with $1.00 min bid price rule.
-
Atossa Q2 operating expenses $9M; FDA clears IND path for (Z)-endoxifen in metastatic breast cancer
Total operating expenses $9.0M in Q2 2025, up 27% YoY from $7.1M; R&D spend rose 55% to $5.5M.
-
Atossa Q1 cash $65.1M; pivots (Z)-endoxifen to metastatic breast cancer
Ended Q1 2025 with $65.1M cash, no debt; no revenue reported.
-
Atossa stockholders elect directors, ratify auditor, approve say-on-pay at 2025 annual meeting
Class I directors Steven C. Quay (28.4M for, 4.2M withheld) and Jonathan F. Finn (30.2M for, 2.4M withheld) elected.
-
Intas Pharmaceuticals challenges two Atossa endoxifen patents with PGR and IPR petitions at USPTO
Intas filed PGR petition against U.S. Patent No. 12,071,391, titled 'Methods for Making and Using Endoxifen'.
-
Atossa Therapeutics ends 2024 with $71.1M cash; advances (Z)-endoxifen for metastatic breast cancer
Cash and equivalents $71.1M, no debt; operating expenses fell to $27.6M from $31.4M in 2023.
-
Atossa to pursue metastatic breast cancer indication; (Z)-endoxifen more than doubled PFS vs tamoxifen (7.2 vs 2.4 mo)
Strategic decision to pursue metastatic breast cancer indication for (Z)-endoxifen, citing potentially faster regulatory path.
-
Atossa receives Nasdaq minimum bid price deficiency notice; compliance period through Aug 20, 2025
Received Nasdaq deficiency notice on Feb 21, 2025 for failing to maintain $1.00 minimum bid price for 30 consecutive business days.
-
PTAB invalidates Atossa's US Patent 11,572,334; new patent 12,201,591 issued
PTAB final decision found all claims of US Patent 11,572,334 unpatentable; Atossa will not appeal.
-
Atossa presents positive PK/tolerability data from Phase 2 EVANGELINE trial of (Z)-endoxifen
50% of patients on 80 mg (Z)-endoxifen + goserelin met target plasma Css of 500-1,000 ng/mL.
-
Atossa Therapeutics enters at-the-market equity facility for up to $100M
Agreement with Jefferies LLC dated Nov 19, 2024 to sell up to $100M of common stock at-the-market.
-
Atossa Therapeutics reports Q3 2024 results, highlights positive Phase 2 data for (Z)-endoxifen
Announced positive topline from KARISMA-Endoxifen Phase 2: MBD reductions of 19.3% (1 mg) and 26.5% (2 mg) vs placebo.
-
Atossa reports positive Phase 2 data for (Z)-endoxifen reducing breast density by up to 26.5%
Relative MBD reduction of 19.3% (1 mg) and 26.5% (2 mg) vs placebo in KARISMA-Endoxifen trial.
-
Atossa reports $79.5M cash, no debt; EVANGELINE Phase 2 40mg cohort shows 100% disease control rate
Ended Q2 2024 with $79.5M cash and cash equivalents, no debt; interest income $1.1M in Q2.
-
Atossa appoints Heather Rees as CFO, increases authorized shares to 360M
Heather Rees appointed CFO effective June 27, 2024; salary set at $439,700 with 40% bonus target.
-
Atossa Q1 2024 net loss $5.9M; EVANGELINE 100% disease control at 24 weeks
Net loss of $5.9M (operating expenses $7.0M, interest income $1.1M); cash $84.0M, no debt.
-
Atossa reports FY2023 results: $88.5M cash, R&D spend up; two Phase 2 trials fully enrolled
Ended FY2023 with $88.5M cash and equivalents, no debt.
-
Atossa ends FY2023 with $88.5M cash; two Phase 2 studies fully enrolled, data due H2 2024
Cash and equivalents $88.5M as of Dec 31, 2023; no debt outstanding.
-
Atossa regains Nasdaq minimum bid price compliance; stock remains listed
Received Nasdaq letter on March 15, 2024 confirming regained compliance with Listing Rule 5550(a)(2).
-
Atossa Therapeutics appoints breast cancer specialist Dr. Tessa Cigler to board
Dr. Cigler is a medical oncologist and clinical investigator at Weill Cornell Breast Center.
-
Atossa Q3 2023: cash $94M; two Phase 2 trials 80% enrolled; net loss details
Cash and cash equivalents $94.0M as of Sept 30, 2023.
-
Atossa Therapeutics appoints Jonathan Finn to board of directors and audit committee
Jonathan Finn appointed to board as Class I director and audit committee member, effective November 9, 2023.
-
Atossa Therapeutics CFO Greg Weaver resigns; Heather Rees appointed as principal financial officer
Greg Weaver resigned as EVP and CFO effective Oct 5, 2023; resignation not due to disagreement with company.
-
Atossa receives Nasdaq deficiency notice for bid price below $1 for 30 days
Nasdaq letter dated September 26, 2023, citing non-compliance with Listing Rule 5550(a)(2) for minimum bid price.
-
Intas Pharmaceuticals files PGR petition challenging Atossa's endoxifen patent
Intas Pharmaceuticals filed a Post-Grant Review petition with USPTO challenging Atossa's U.S. Patent No. 11,572,334.
-
Atossa Therapeutics Q2 2023 net loss $9.8M; clinical enrollment milestones; CFO appointed
Cash at June 30, 2023: $99.4M, down from $110.9M at Dec 31, 2022.
-
Atossa Therapeutics regains Nasdaq compliance with minimum bid price requirement
Received Nasdaq notice on July 13, 2023 that it regained compliance with Listing Rule 5550(a)(2).
-
Atossa Therapeutics authorizes $10M stock repurchase program through Dec 31, 2023
Board approved repurchase of up to $10M of common stock through December 31, 2023.
-
Atossa receives Nasdaq non-compliance notice for independent director majority rule
Received notice on June 21, 2023 for failing Nasdaq Listing Rule 5605(b)(1) requiring majority independent directors.
-
Atossa appoints Greg Weaver as CFO, succeeding Kyle Guse effective June 1, 2023
Greg Weaver appointed EVP and CFO effective June 1, 2023, succeeding Kyle Guse who ceased as of May 26, 2023.
-
Atossa Therapeutics dismisses BDO, appoints Ernst & Young as new auditor
On May 17, 2023, Atossa dismissed BDO USA LLP as independent auditor; no accounting disagreements.
-
Atossa Q1 2023: cash $103.9M, no debt; Phase 2 trials initiated/expanded
Ended Q1 2023 with $103.9M cash and cash equivalents, zero debt.
-
Atossa Therapeutics reports 2023 annual meeting vote results; all proposals passed
Elected directors: Galli with 15,993,221 for, Steinhart with 22,292,391 for; broker non-votes ~30M.