28 stories on the wire
Regulatory
28 filings Chronological · ET
NFE
NEW FORTRESS ENERGY Recapitalizes With 1-for-50 Reverse Split
An amended charter effective September 11, 2026 combines every 50 Class A shares into one, wipes out Class B stock and creates mandatorily convertible preferred.
a day ago
PRO
KPTI
KARYOPHARM Strikes Forbearance Deal With Lenders and Noteholders
Karyopharm signed a forbearance agreement and limited waiver covering its term loan, both 9.00% convertible note series and its royalty financing.
a day ago
PRO
CNI
CN Files Midwest Access Conditions in UNION PACIFIC-Norfolk Southern Merger Review
CN told the Surface Transportation Board it will seek trackage rights and yard access in Kansas City, St. Louis and Illinois as a merger remedy.
a day ago
PRO
WRD
WERIDE Wins Spain's First National Permit for Level 4 Robotaxis
WeRide, Uber and fleet operator AVOMO received Spain's first national Level 4 autonomous passenger vehicle permit, targeting a commercial Madrid launch by end-2026.
2 days ago
PRO
WRD
WERIDE and Uber Win Spain's First National Level 4 Robotaxi Permit
Spain's traffic authority cleared WeRide, Uber and fleet operator AVOMO to prepare a driverless service in Madrid, with commercial rides targeted by end-2026.
2 days ago
PRO
INBS
INTELLIGENT BIO SOLUTIONS Files FDA 510(k) for Fingerprint Drug Test
INBS submitted its 510(k) premarket notification for codeine detection with its fingerprint sweat screening system, backed by studies showing 100% specificity.
3 days ago
PRO
IVDA
IVEDA Wins Second 180-Day Nasdaq Extension on $1 Bid Price
Iveda has until March 1, 2027 to close above $1.00 for ten straight sessions and says a reverse split remains one option.
3 days ago
PRO
QBTS
D-WAVE QUANTUM Hands US Commerce Department an Equity Stake for CHIPS Award
D-Wave agreed to issue common stock to the US Department of Commerce at $14.093 per share as an inducement for a CHIPS Act award signed on September 4, 2026.
3 days ago
PRO
QNRX
FDA Grants QUOIN PHARMACEUTICALS Second Rare Pediatric Tag for QRX003
Quoin's lead asset QRX003 receives Rare Pediatric Disease Designation for Peeling Skin Syndrome, opening the door to a second Priority Review Voucher.
4 days ago
PRO
ABAT
AMERICAN BATTERY TECHNOLOGY Clears BLM Hurdle for Tonopah Flats Lithium
The Bureau of Land Management accepted the mine and refinery Plan of Operations for ABTC's Nevada lithium project, moving it into environmental review.
4 days ago
PRO
GFS
GLOBALFOUNDRIES to Issue 9.9M Shares to U.S. Commerce Department
GlobalFoundries will hand the Commerce Department nearly 9.91 million ordinary shares at $37.85 apiece, a stake worth roughly $375 million.
4 days ago
PRO
DFTX
FDA Grants DEFINIUM Second Breakthrough Therapy Tag for LSD Tablet
Definium's DT120 gets Breakthrough Therapy designation in major depressive disorder after a Phase 3 win, adding to an earlier tag in generalized anxiety.
4 days ago
PRO
AZN
FDA Approves ASTRAZENECA Breast Cancer Drug Etcamah for First-Line Use
Accelerated US approval of camizestrant with a CDK4/6 inhibitor rests on SERENA-6, which cut the risk of progression or death by 56%.
4 days ago
PRO
QBTS
D-WAVE Signs $100M CHIPS Act Award With Commerce Department
D-Wave Quantum has entered a $100 million Other Transaction Agreement with the U.S. Department of Commerce to prototype scalable superconducting quantum components.
4 days ago
PRO
POMRY
POMMERY Auditors Flag Material Going-Concern Doubt in 2025 Filing
The Champagne group's 2025 registration document carries an auditor paragraph on material uncertainty over its ability to continue as a going concern.
4 days ago
PRO
Regulatory
PHARMA EQUITY GROUP Faces Court Challenge to EUR 10.5M Arbitral Award
Interpatium has asked a Danish district court to set aside the June 2026 arbitration ruling that ordered it to pay Pharma Equity Group EUR 10.5 million.
5 days ago
PRO
GURE
GULF RESOURCES Files 8-K on Nasdaq Listing Deficiency
The Shandong-based chemicals producer disclosed an Item 3.01 notice covering delisting or failure to satisfy a continued listing rule.
8 days ago
PRO
QNCX
QUINCE THERAPEUTICS Files 8-K Flagging Listing Rule Issue
The biotech filed an Item 3.01 disclosure with the SEC covering a delisting notice or failure to meet a continued listing standard, dated August 31, 2026.
8 days ago
PRO
SNTI
SENTI BIOSCIENCES Files Amended Terms for Senior Secured Convertible Notes
An 8-K discloses a revised form of senior secured convertible note maturing November 23, 2026, repayable in cash at 200% of outstanding principal.
8 days ago
PRO
DPU
TOP KINGWIN Holders Approve 1-for-50 Reverse Split and Nexpu Name Change
Shareholders backed a 200x supervoting Class B structure, a jump in authorized capital to $625 million and a share consolidation effective December 17, 2026.
8 days ago
PRO
IONS
FDA Approves IONIS Drug Zanvastro for Alexander Disease
Ionis wins first-ever approval for a disease-modifying Alexander disease therapy, plus a rare pediatric disease priority review voucher.
8 days ago
PRO
NLST
NETLIST Loses Three Federal Circuit Appeals Against Micron on Same Day
The Federal Circuit affirmed PTAB rulings invalidating claims of five Netlist memory patents challenged by Micron, including one precedential decision.
9 days ago
PRO
AUGO
Aura Minerals Director Sells $10.4 Million of Shares in Open Market
A Form 4 shows director Bruno Sousa Mauad sold 127,500 Aura Minerals shares at $81.20 apiece on Aug. 31, cutting his stake by more than 40%.
10 days ago
PRO
ABT
FDA Authorizes First Dual Glucose and Ketone Wearable, Abbott's Libre Duo
The FDA cleared the Libre Duo 10 Day Continuous Dual Glucose Ketone Monitoring System for people with diabetes aged 2 and older.
10 days ago
PRO
RVMD
FDA Approves Rasonque, First RAS Inhibitor for Metastatic Pancreatic Cancer
The FDA cleared daraxonrasib for the most common form of advanced pancreatic cancer, acting months ahead of its review deadline.
10 days ago
PRO
ROIV
FDA Approves Lisraya, First Oral Drug for Dermatomyositis in Adults
The FDA has cleared Lisraya (brepocitinib) tablets, the first oral therapy specifically indicated for adults with dermatomyositis.
10 days ago
PRO
PTGX
FDA Approves Mimrylo (Rusfertide), First Hepcidin Mimetic for Polycythemia Vera
The FDA has cleared Mimrylo (rusfertide) for adults with polycythemia vera, calling it the first drug of its kind for the rare blood disorder.
10 days ago
PRO
BRLS
Borealis Foods Gets Nasdaq Deficiency Notice Over Late Q2 10-Q
Borealis Foods says a review of the accounting treatment of its Conversion Agreement delayed its second-quarter report, triggering a Nasdaq compliance notice.
10 days ago
PRO
No filings match.Try another ticker or clear the filter.