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Cerebras CEO says chipmaker's 'aspiration' is to hold IPO in 2025

Cerebras CEO says chipmaker's 'aspiration' is to hold IPO in 2025

CNBC16-05-2025

Cerebras CEO Andrew Feldman said his hope is to take his company public in 2025 now that the chipmaker has obtained clearance from the U.S. government to sell shares to an entity in the United Arab Emirates.
"That's our aspiration," Feldman told reporters on Thursday at the company's Supernova conference in San Francisco, after being asked if an IPO was likely this year.
Cerebras, which makes processors for artificial intelligence workloads, filed to go public in September but hasn't provided an update on the expected size or timing of an offering. In March, the company said it had obtained clearance from a U.S. committee to sell shares to Group 42, a Microsoft-backed AI company based in the UAE.
That clearance came from the Committee on Foreign Investment in the United States, or CFIUS, and marked a key step for Cerebras in its effort to go public. Cerebras competes with Nvidia, whose graphics processing units (GPUs) are the industry's choice for training and running AI models. More than 85% of Cerebras' revenue in the first half of 2024 came from Group 42.
The tech IPO market broadly has been in a drought since early 2022, when rising inflation and higher interest rates pushed investors out of risky assets. Cerebras appeared poised to be the first notable pure-play AI IPO after its filing, but then the came the delay. CoreWeave, which provides AI infrastructure, debuted in March and has seen its market value jump about 65% since its IPO.
The IPO market is showing signs of life, with trading app eToro hitting the Nasdaq this week and digital health provider Hinge Health scheduled to go out next week.
The Middle East is becoming a more critical market for AI development.
Nvidia CEO Jensen Huang was in Riyadh, Saudi Arabia this week along with other tech leaders and President Donald Trump for the Saudi-U.S. Investment Forum. Nvidia said at the event that it will sell more than 18,000 of its latest AI chips to Saudi company Humain.
Group 42 is also reportedly on tap to purchase 100,000 GPUs a year as part of a bigger agreement between the U.S. and UAE.
Feldman said at the roundtable with reporters that it's "important to be among the big dogs" and said, regarding the latest announcements, "You've got half the story. I can't share the other half."
In addition to Microsoft, Cerebras sells to Meta and IBM. Feldman said last year that the company would have another "hyperscaler" within the first half of 2025.
"We're close with another," he said on Thursday. "I think they haven't been the quickest to respond."
Earlier in the day, Cerebras announced the ability to run an open-source model from Alibaba on its chips at what it says is a lower price than what OpenAI's GPT-4.1 model charges, and at a higher speed.

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Allogene Therapeutics Provides Updated Phase 1 Data Highlighting Durable Responses with ALLO-316 in Heavily Pretreated Advanced Renal Cell Carcinoma at ASCO
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Allogene Therapeutics Provides Updated Phase 1 Data Highlighting Durable Responses with ALLO-316 in Heavily Pretreated Advanced Renal Cell Carcinoma at ASCO

Data Highlights Transformative Promise of CAR T in Solid Tumors Phase 1 Trial with ALLO-316 Demonstrated Potential to Provide Meaningful Clinical Benefit in Patients with CD70 TPS ≥ 50% Advanced or Metastatic RCC A Single Dose of ALLO-316 Achieved a 31% Confirmed Response Rate Four of Five Confirmed Responders Remain in Response Including One Ongoing Remission Over 12 Months Robust Expansion, Persistence, and Tumor Infiltration of ALLO-316 Seen with Standard Lymphodepletion, Showcasing Dagger® Technology as a Next-Generation Allogeneic Platform Phase 1 Safety Profile was Manageable; Proactive Diagnostic and Management Strategies Proved Effective in Mitigating IEC-HS While Preserving Efficacy SOUTH SAN FRANCISCO, Calif., June 01, 2025 (GLOBE NEWSWIRE) -- Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company pioneering the development of allogeneic CAR T (AlloCAR T™) products for cancer and autoimmune disease, presented updated data from the Phase 1 TRAVERSE study of ALLO-316 in renal cell carcinoma (RCC) during an oral presentation at the 2025 ASCO Annual Meeting. The Phase 1 TRAVERSE trial enrolled patients with advanced or metastatic renal cell RCC. Leveraging the proprietary Dagger® technology to enable robust CAR T cell expansion, it stands as the first and only allogeneic CAR T product to show promise in treating solid tumors. The presentation focused on the Phase 1b expansion cohort from the Phase 1 TRAVERSE study in which patients were treated with a standard regimen of cyclophosphamide and fludarabine followed by a single dose of 80 million AlloCAR T™ cells. 'ALLO-316 is showing clear evidence of targeted antitumor activity in patients who had failed most or all approved therapies for advanced or metastatic renal cell carcinoma,' said Zachary Roberts, M.D., Ph.D., EVP, Research and Development and Chief Medical Officer at Allogene. 'Our proprietary Dagger technology allows the use of a standard cyclophosphamide and fludarabine-based lymphodepletion regimen with a single dose of ALLO-316. Strong CAR T-cell kinetics and extensive infiltration of tumor tissue by CAR T cells are combining to generate deep and durable remissions. These are results that were previously considered out of reach for patients with advanced solid tumors.' 'Patients diagnosed with advanced or metastatic renal cell carcinoma often face a median survival in months after exhausting standard therapies,' said Samer A. Srour, MB ChB, MS, Associate Professor of Stem Cell Transplantation and Cellular Therapy at The University of Texas MD Anderson Cancer Center and lead investigator of the TRAVERSE trial. 'These updated results from a larger cohort of patients with confirmed CD70 positive tumors provide compelling evidence that treatment with ALLO-316 can reduce tumor burden, control disease, and in some cases deliver durable responses. These findings underscore the clinical promise of an allogeneic CAR T to address the significant unmet needs in solid tumors and offer hope to patients who have exhausted other options.' In the Phase 1b expansion cohort, 22 patients whose tumors had progressed on multiple prior therapies were treated with lymphodepletion and 20 were treated with ALLO-316. All patients had tumors resistant to immune checkpoint blockers and at least one tyrosine kinase inhibitor (TKI), 82% had ≥2+ prior TKI, and 41% had prior belzutifan. 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TEAEs ≥20% incidence in Phase 1b, n (%) Phase 1b (N=22a) All Grades Grade ≥3 Neutropenia 15 (68) 15 (68) White blood cell count decreased 15 (68) 15 (68) Anemia 13 (59) 9 (41) Thrombocytopenia 12 (55) 6 (27) Nausea 8 (36) 0 ALT increased 7 (32) 2 (9) Peripheral edema 7 (32) 0 Pyrexia 7 (32) 0 Arthralgia 6 (27) 0 AST increased 6 (27) 2 (9) Fatigue 5 (23) 0 Headache 5 (23) 0 AEs of Special Interest Any Grade Grade ≥3 CRS 15 (68) 0 Infection 10 (45) 8 (36) IEC-HS 8 (36) 2 (9)b ICANS 4 (18) 0 Graft-versus-host disease 0 0 IEC-HS includes the preferred terms immune effector cell-associated HLH-like syndrome and Hemophagocytic lymphohistiocytosis. a Includes 2 patients who received LD but did not receive ALLO-316 b One patient experienced G4 IEC-HS based on GI bleeding with subsequent improvement and 1 patient experienced G3 IEC-HS based on hypotension managed without pressors with subsequent improvement. 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About Allogene TherapeuticsAllogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of 'off-the-shelf' CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. For more information, please visit and follow @AllogeneTx on X and LinkedIn. Cautionary Note on Forward-Looking Statements for Allogene This press release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. This press release may, in some cases, use terms such as 'develop,' 'potential,' 'expect,' 'can,' 'enable,' 'showing,' 'generate,' 'may,' 'could,' 'designed to,' 'promise,' 'hope,' 'ongoing,' 'indicating,' 'mitigate,' 'evaluate,' 'pioneer,' 'goal' or 'will,' including alternative forms thereof, or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. 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The 8.1% return this week takes Oportun Financial's (NASDAQ:OPRT) shareholders one-year gains to 97%
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Insiders' US$15.9m Investments In Red Following Shineco's US$5.3m Dip In Market Value
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