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ContextLogic Inc. (LOGC) reported its Q3 2024 financial results, showing a significant improvement with a net loss of $1 million compared to $80 million in Q3 2023. The company maintains a strong liquidity position with $33 million in cash, $117 million in marketable securities, and $8 million in other current assets. Operating with 8 full-time employees, the company incurred $3 million in general and administrative expenses and earned $2 million in interest income. ContextLogic projects to end fiscal 2024 with approximately $155 million in combined cash, securities, and restricted cash, while maintaining low total liabilities of $5 million as it continues to evaluate strategic opportunities.
ContextLogic Inc. (Nasdaq: LOGC) reported its Q2 2024 financial results following the sale of its Wish platform and related assets to Qoo10 Inc. on April 19, 2024. Key highlights include:
- Net loss of $13 million, compared to $80 million in Q2 2023
- $103 million in cash and cash equivalents
- $47 million in marketable securities
- $13 million in general and administrative expenses
- $2 million in interest income
The company now focuses on identifying strategic opportunities to utilize its NOLs and build shareholder value. ContextLogic projects to end 2024 with approximately $155 million in cash, cash equivalents, marketable securities, and restricted cash.
Alexion, AstraZeneca Rare Disease has completed its acquisition of LogicBio Therapeutics, Inc. (NASDAQ: LOGC), enhancing its capability in genomic medicine. This strategic move leverages LogicBio's unique technology and experienced R&D team, facilitating growth in rare disease therapeutics. The acquisition was finalized on November 16, 2022, following a successful tender offer. LogicBio shareholders will receive $2.07 per share. Frederic Chereau, the CEO of LogicBio, will transition to a senior role within Alexion.
LogicBio Therapeutics (NASDAQ: LOGC) reported Q3 2022 financial results on November 14, revealing revenue of $2.7 million, up from $2.1 million in Q3 2021. The net loss narrowed to $5.8 million ($0.18 per share) from a $10.2 million loss in the prior year. Key updates include interim data from the SUNRISE trial for LB-001 in pediatric MMA patients, demonstrating increased ALB-2A levels, indicating gene editing success. Additionally, a merger agreement with Alexion, at $2.07 per share, is set to close within six weeks, pending shareholder approvals.
Alexion, AstraZeneca Rare Disease, has announced its definitive agreement to acquire LogicBio Therapeutics (NASDAQ: LOGC) for $2.07 per share. This acquisition aims to enhance Alexion's capabilities in genomic medicine by leveraging LogicBio's unique gene delivery and editing technologies, as well as its experienced R&D team. The deal, approved by both boards, is expected to close within four to six weeks, pending shareholder approval. This strategic move underscores Alexion's commitment to advancing treatments for rare genetic diseases.
LogicBio Therapeutics (NASDAQ: LOGC) announced a definitive agreement for its acquisition by AstraZeneca Rare Disease. The agreement involves a cash tender offer of $2.07 per share, approved unanimously by both boards. This acquisition aims to enhance AstraZeneca's capabilities in genomic medicine by integrating LogicBio's technology and experienced R&D team. The deal is projected to close in four to six weeks, pending the tender of at least a majority of shares. Both companies expect to leverage this collaboration to advance treatments for rare genetic diseases.
LogicBio Therapeutics (LOGC) announced promising preclinical results for mLB-001, a gene therapy for methylmalonic acidemia (MMA), published in PLOS ONE. The study demonstrated that a single administration of mLB-001 prevented severe weight loss and mortality in MMUT deficient mice subjected to a high protein diet. This approach shows potential for pediatric patients currently reliant on strict dietary management. The results support the ongoing development of LB-001, aimed at addressing the underlying causes of MMUT deficiency.
LogicBio Therapeutics (LOGC) reported interim data from the SUNRISE trial, showing detectable ALB-2A biomarkers in four pediatric patients indicating gene insertion success. Notably, two patients exhibited increasing ALB-2A levels, suggesting the expansion of edited cells. The proprietary mAAVRx manufacturing process demonstrated a 15-30 fold yield increase compared to standard methods. Financially, LOGC generated $3.2 million in collaboration revenue for Q2 2022, up from $0.8 million in Q2 2021, while net loss decreased to $5.0 million from $10.5 million year-over-year, with cash reserves of $38.8 million.
LogicBio Therapeutics, Inc. (Nasdaq: LOGC) announced that CEO Frederic Chereau will present an overview at the H.C. Wainwright Global Investment Conference from May 23-26, 2022. The pre-recorded presentation will be available for on-demand viewing starting May 24, 2022, at 7:00 a.m. ET. A webcast of the presentation can be accessed on the company's website and will be available for approximately 30 days.
LogicBio focuses on genetic medicine, developing innovative genome editing and gene delivery platforms to address rare diseases.
LogicBio Therapeutics (NASDAQ: LOGC) announced the lifting of the FDA clinical hold on its SUNRISE trial for LB-001, a therapy for pediatric patients with methylmalonic acidemia (MMA). The company plans to resume patient dosing in Q3 2022, with interim clinical data expected by the end of Q2 2022. Financial results for Q1 2022 showed revenue of $2.8 million, an increase from $0.5 million in Q1 2021. R&D expenses decreased to $5.6 million from $6.4 million. The net loss narrowed to $6.7 million, or $0.20 per share, compared to a loss of $10.3 million, or $0.32 per share, in the previous year.
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