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Nasdaq Composite Falls 1.3% as Tech Stocks Struggle
S&P 500 slipped for the second consecutive day while losses on the tech-dominant Nasdaq Composite accelerated, with the index finishing lower by 1.3% on Thursday. Technology was by far the worst-performing sector in the benchmark S&P as AI buildout theme was thumped by a Financial Times report, stating that OpenAI's annualized revenues were closer to $50B at the end of September - well below the $70B figure previously circulated. Micron, Sandisk, Intel, Broadcom, Seagate, AMDand Oraclewere among the 20 worst stocks in the S&P 500, with losses of at least 4%. Meanwhile, software and IT services stocks such as Accentureand Gartner- names viewed to be most exposed to AI disruption - rallied by at least 5%.In the opening hour of the evening session, S&P e-minis and Nasdaq 100 contracts are up a decimal. In commodities, WTI Crude Oil was off the highs but still above $91 per barrel. Energy prices rallied sharply this morning on reports that U.S. may conduct heavy strikes on Iran before the US midterm elections.Check out this evening's top movers from around Wall Street, compiled by The Fly.HIGHER AFTER EARNINGS -Park Aerospace Corp.up 2.7%Oil-Dri Corporation of Americaup 1.0%ALSO HIGHER -XORTX Therapeuticsup 23.9% as company outlines anticipated clinical trial application for XRx-026Humanaup 12.7%, Clover Healthup 10.9% after CMS published 2027 MA - Medicare Part C - and Part D Star RatingsGinkgo Bioworks Holdings, Inc.up 1.0% after announcing it will provide autonomous lab access to NSF X-Labs researchersLOWER -AT&Tdown 6.6%, T-Mobiledown 6.6%, Verizondown 6.2% following announcement by SpaceXthat it has acquired a nationwide low-band spectrum license portfolio of up to 14 megahertz of paired spectrum in the 800 MHz band.Alignment Healthcaredown 23.1%, CVS Healthdown 3.1%, Cignadown 1.8%, Elevance Healthdown 1.6% after CMS published 2027 MA - Medicare Part C - and Part D Star RatingsBraemar Hotels & Resortsdown 3.3% after FY27 guidanceAmerican Expressdown 1.8% after announcing consent to Federal Reserve and OCC compliance orders
Xortx Therapeutics Submits CTA for XRx-026 Clinical Trial
Xortx Therapeutics provided an outline of its anticipated clinical trial application, or CTA, submission to Health Canada for the XRx-026 gout program. The filing supports the company's planned two-part clinical study, XRX-OXY-102, evaluating XORLO, the company's proprietary formulation of oxypurinol, a xanthine oxidase inhibitor, for the treatment of gout. Conducting the first part of the XRX-OXY-102 clinical study in Canada is expected to enable the company to accelerate the delivery of key clinical data in support of its planned new drug application, or NDA, filing with the FDA for marketing approval. Recent drug development team activities have included parallel preparation of the CTA for filing with Health Canada. The application describes the Company's clinical development plan for XRx-026 and its intention to advance the program toward regulatory approval in Canada in parallel with its planned NDA filing with the FDA. Part one of the XRX-OXY-102 clinical trial builds upon the previously reported clinical results for the proprietary XORLO formulation and extends characterization of the commercial tablet form. As the XRx-026 program has advanced, the company has received increased inquiries from potential commercialization partners in a number of jurisdictions. The company has not entered into any agreement with any such party, and there can be no assurance that any of these discussions will result in a transaction.
Xortx Therapeutics Launches Drug Production to Support XRx-026 Program
Xortx Therapeutics announced the launch of production of drug material and tablet manufacturing to support the company's XRx-026 program for the treatment of gout. This manufacturing supports a planned two-part clinical study of Xorlo, the company's proprietary formulation of oxypurinol, a xanthine oxidase inhibitor. The clinical trial, XRX-OXY-102, is being advanced based on prior clinical trial results and discussions with the FDA.
Xortx Therapeutics Terminates Investor Relations Agreement with IR Agency
Xortx Therapeutics terminated its previously announced investor relations and marketing agreement dated May 13 with IR Agency LLC. The IR agreement had a 90-day term commencing May 18 and provided for 10 individual marketing days of news distribution campaigns for an aggregate fee of $2.5M, payable in advance. The fee was fully earned upon receipt and non-refundable. Under the mutual agreement of the parties, the arrangement has been rescinded, all services contemplated under the agreement have been discontinued and the funds previously paid to IR Agency LLC in connection with the agreement were returned to the company on August 14. The original arrangement was disclosed in connection with the Company's $5M public offering completed on May 19. A portion of the offering proceeds, in an amount equal to $2.5M, had been allocated to IR Agency LLC for marketing and advertising services. The company has elected to postpone the investor relations and marketing program while it completes its previously announced voluntary delisting from the TSX Venture Exchange. The Company expects the voluntary delisting to take effect on September 1, 2026, subject to final approval by the TSXV.
Xortx Therapeutics Appoints Mika Grasso as Co-CEO
Xortx Therapeutics announced the addition of Mika Grasso as co-CEO responsible for finance and public markets. Grasso has served as a director of the company since March 24. Grasso has served as an investment manager at a family office, where he has been responsible for sourcing and evaluating the fund's direct investment and co-investment efforts.
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