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Fundamental Global Inc. (NASDAQ: FGF) announced the formation of FG CVR Trust, a Delaware statutory trust, offering a special distribution to common shareholders. Shareholders of record as of August 8, 2025 will receive non-transferable Contingent Value Rights (CVRs), including an initial cash distribution of $10.00 per share expected in September 2025.
The CVR Trust, with assets valued at over $30.00 per common share, will distribute additional cash or in-kind securities as legacy assets are monetized. The company, soon to be renamed FG Nexus Inc., will retain approximately $5.00 per share in NAV and is undergoing a strategic transformation with a $200 million private placement to implement an Ethereum Treasury Strategy.
- Initial cash distribution of $10.00 per share to shareholders
- CVR Trust assets valued at over $30.00 per common share
- $200 million private placement secured for strategic transformation
- Company retaining $5.00 per share in NAV for new blockchain strategy
- CVRs are non-transferable, limiting shareholder flexibility
- Timeline for additional distributions beyond initial payment remains uncertain
- Future distributions dependent on successful monetization of legacy assets
Tenon Medical (NASDAQ:TNON) has acquired sacroiliac joint-specific assets from SiVantage, including their SImmetry庐 and SImmetry+鈩� technologies. The strategic acquisition transforms Tenon into a multi-product, multi-approach sacro-pelvic organization, expanding its portfolio across multiple approaches to sacro-pelvic anatomy.
The transaction brings critical technologies, intellectual property, and key leadership to Tenon, with SiVantage's co-founders joining as Chief Innovations Officer and Chief Commercial Officer. The deal structure includes an upfront cash component and equity issuance, with most consideration tied to future performance milestones. Integration is expected to complete in Q4 2025.
The acquisition immediately strengthens Tenon's product pipeline and is expected to contribute to revenue, supported by extensive clinical data demonstrating safety and performance in sacroiliac joint fusion procedures.
- Immediate revenue contribution expected from acquired core technology products
- Acquisition brings extensive clinical data and proven safety record
- Strategic addition of experienced leadership with SiVantage co-founders joining executive team
- Expanded product portfolio across multiple approaches to sacro-pelvic anatomy
- Performance-based deal structure minimizes upfront financial risk
- Potential share dilution from equity issuance component of transaction
- Integration risks and costs through Q4 2025
- Additional cash expenditure required for upfront payment
Erayak Power Solution Group (NASDAQ: RAYA), a power supply industry manufacturer, has successfully closed its previously announced registered direct offering, raising approximately $7 million in gross proceeds. The offering involved the sale of 107,692,307 Class A ordinary shares at $0.065 per share.
The transaction included pre-funded warrants with a purchase price of $0.065 less the $0.0001 exercise price per share. Craft Capital Management LLC served as the sole placement agent, with legal representation from Ortoli Rosenstadt LLP for Erayak and Sichenzia Ross Ference Carmel LLP for Craft Capital.
- Secured $7 million in gross proceeds to strengthen financial position
- Successfully completed registered direct offering with institutional investors
- Utilized existing shelf registration statement, streamlining the offering process
- Significant dilution potential with 107.7 million new shares
- Low share price of $0.065 indicates challenging market conditions
- Additional expenses for placement agent fees and offering costs will reduce net proceeds
Brown & Brown (NYSE:BRO) has successfully completed its previously announced acquisition of RSC Topco, the holding company for Accession Risk Management Group. The acquisition strengthens Brown & Brown's position as a leading insurance brokerage firm.
Following the acquisition, Brown & Brown now operates across more than 700 locations with a workforce exceeding 23,000 professionals. The company continues to focus on delivering comprehensive insurance solutions and specialized services to its customers.
- Expansion of Brown & Brown's market presence with 700+ locations
- Enhanced workforce capacity with over 23,000 professionals
- Strategic acquisition strengthening insurance brokerage capabilities
- None.

Pheton Holdings (NASDAQ:PTHL), a healthcare solution provider specializing in brachytherapy treatment planning systems, has issued an official statement addressing recent market volatility and misleading rumors. The company's stock experienced a significant decline following a speculative article published by The Bear Cave on July 29, 2025.
The company categorically denies any involvement in stock price manipulation or rumors regarding a potential acquisition by Gilead Sciences. Pheton confirms it has had no contact with Gilead and plans to engage with Nasdaq and regulatory bodies to address the situation. Management emphasizes its commitment to transparency and maintaining strong corporate governance standards.
- None.
- Share price experienced extraordinary and unexpected decline
- Company subject to potentially damaging speculative article questioning stock activity
- Potential market manipulation affecting company's stock
T-Mobile (NASDAQ: TMUS) has completed its acquisition of UScellular's wireless operations for approximately $4.3 billion, consisting of $2.6 billion in cash and $1.7 billion in assumed debt. The deal brings over 4 million UScellular customers into T-Mobile's network, providing them access to enhanced coverage and new benefits.
The transaction includes UScellular's wireless customers, stores, and specific spectrum assets. T-Mobile also completed the Iowa Transactions for an additional $175 million. The UScellular brand will transition to T-Mobile in phases, while Array Digital Infrastructure Inc. (formerly UScellular) will retain ownership of significant spectrum and tower assets.
Starting August 7, UScellular customers will gain access to T-Mobile's dining and travel benefits, with future access to unlimited plans featuring Netflix, AppleTV+, MLB.TV, international roaming, and in-flight Wi-Fi benefits.
- Acquisition adds over 4 million new customers to T-Mobile's network
- Expands network coverage and improves service in UScellular's footprint
- Provides high-speed connectivity access to hundreds of thousands of new households
- Nearly all UScellular customer devices will remain compatible with T-Mobile's network
- Transaction maintains T-Mobile's $14 billion shareholder return authorization for 2025
- Significant acquisition cost of $4.3 billion including $2.6 billion cash payment
- Additional $175 million spent on Iowa Transactions
- Assumption of $1.7 billion in debt through exchange offer

ATA Creativity Global (NASDAQ:AACG) has signed a significant MOU with Baby BTC Strategic Capital Limited, a fund backed by the Babylon Foundation. The deal includes a $30 million subscription for new shares and $70 million in warrants, totaling a potential $100 million investment. Upon completion, Baby Capital will gain control of AACG and appoint three directors.
The strategic partnership aims to expand Bitcoin staking business through Babylon's innovative Layer 2 network technology, which has already attracted over 57,000 Bitcoins ($5 billion in staking value). AACG plans to implement a "strategic reserve treasury" approach, primarily investing in Baby tokens and partially in Bitcoin, with plans for continuous acquisition through PIPE, ATM, and convertible bond issuances.
- None.
- Complete change in business control and board restructuring
- High concentration risk in Baby tokens with current market cap under $100M
- Significant business model pivot from current operations
- Substantial dependency on Babylon's technology and ecosystem

BioXcel Therapeutics (Nasdaq: BTAI) has completed the last patient visit in its pivotal Phase 3 SERENITY At-Home clinical trial, evaluating IGALMI庐 (dexmedetomidine) for treating agitation in bipolar disorders or schizophrenia patients at home. The study collected data from over 2,200 agitation episodes across more than 200 patients at 22 sites nationwide.
The double-blind, placebo-controlled trial tested a 120 mcg dose of BXCL501 and aims to support a supplemental New Drug Application (sNDA) to expand IGALMI's label for outpatient use. Topline data is expected this month. If approved, IGALMI would become the first FDA-approved therapy for the estimated 23 million annual episodes of bipolar or schizophrenia-related agitation occurring at home in the U.S.
- Study completion marks significant milestone towards potential FDA approval for at-home use
- Large dataset collected with over 2,200 agitation episodes
- Well-distributed patient enrollment across 22 sites with no site bias
- Addresses large unmet need with 23 million annual agitation episodes occurring at home
- Topline data results not yet available
- FDA approval for at-home use still pending
- Currently no approved therapies in this setting, indicating potential regulatory challenges

Exicure (Nasdaq: XCUR) has completed the last patient visit in its Phase 2 clinical trial evaluating GPC-100 (burixafor) for stem cell mobilization in multiple myeloma patients. The study assesses GPC-100's ability to improve CD34+ hematopoietic stem cell mobilization for autologous stem cell transplant (ASCT).
Key highlights include GPC-100's differentiated rapid mobilization time of just 45 minutes before collection, compared to traditional overnight procedures. The company expects topline results in Q4 2025. Beyond multiple myeloma, Exicure plans a Phase 1 study in acute myeloid leukemia and is exploring potential collaborations for cell and gene therapy applications.
- GPC-100 demonstrates rapid stem cell mobilization in just 45 minutes vs traditional overnight procedures
- Successful completion of Phase 2 trial last patient visit
- Potential expansion into AML and cell/gene therapy applications
- Positive differentiation from current treatment options based on ASH 2024 data
- Topline results not yet available
- Phase 2 trial still requires data analysis and regulatory review