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Fulgent Genetics, Inc. (NASDAQ: FLGT) is a technology-driven company specializing in genetic testing, with the mission of making advanced genetic diagnostics accessible and affordable. Founded in 2011, Fulgent Genetics focuses on providing flexible and comprehensive genetic testing solutions aimed at improving everyday lives. The company operates through two primary segments: laboratory services and therapeutic development.
The laboratory services segment, which is the main revenue generator, includes technical laboratory services and professional interpretation of laboratory results by licensed physicians. Fulgent Genetics offers a broad array of tests that cover various genetic disorders, helping clinicians and patients obtain clinically actionable diagnostic information.
The therapeutic development segment is dedicated to creating drug candidates for a broad range of cancers. Utilizing innovative nanoencapsulation and targeted therapy platforms, Fulgent aims to improve the pharmacokinetic profile and therapeutic window of new and existing cancer drugs.
One of the company's recent achievements is a partnership with CooperSurgical, enabling the addition of exclusive newborn genetic screening panels to the services offered by Cord Blood Registry® (CBR®), the largest private newborn stem cell preservation company globally.
Fulgent's Picture® Genetics, launched in 2019, provides consumers direct access to comprehensive genetic testing at home. The tests cater to various needs and offer clinically actionable, medical-grade results with professional oversight. This complements Fulgent's laboratory services by making genetic testing more accessible and user-friendly.
With its headquarters in El Monte, California, Fulgent Genetics continues to expand its reach, serving clients both in the United States and internationally. The company's commitment to excellence is reflected in its collaborations with top clinicians and continuous improvements to its testing panels and report formats.
Fulgent Genetics (NASDAQ: FLGT) reported Q3 2024 financial results with total revenue of $71.7 million, representing a 9% year-over-year growth in core revenue. The company posted a GAAP loss of $14.6 million (-$0.48 per share) and non-GAAP income of $9.4 million ($0.31 per share). The company maintains strong liquidity with $815.4 million in cash and investments.
Fulgent reiterates its full-year 2024 core revenue guidance of $280 million and improves its GAAP loss guidance from -$1.95 to -$1.70 per share. The company also revised its non-GAAP outlook from a loss of $0.30 per share to an income of $0.33 per share.
Fulgent Genetics (NASDAQ:FLGT) has announced its management team's upcoming participation in two major healthcare conferences. The company will present at the UBS Global Healthcare Conference on November 12th at 2:45 PM Pacific Time and the Piper Sandler 36th Annual Healthcare Conference on December 4th at 11:30 AM Eastern Time.
Live webcasts of both presentations will be available on Fulgent's Investor Relations website, with replay options accessible approximately one hour after each event concludes.
Fulgent Genetics (NASDAQ: FLGT) has secured a five-year contract worth up to $99M from the U.S. Department of Veterans Affairs to provide hereditary cancer and pharmacogenetic testing to Veterans. The company, which has been offering genetic testing services to VA members since 2017, will expand its services to include hereditary cancer tests for individuals with cancer or family history of certain cancers. The contract also covers pharmacogenetic testing, which uses genomic information to determine medication responses. Fulgent's comprehensive suite of germline tests enables custom solutions, utilizing next-generation sequencing for higher resolution and greater coverage.
Fulgent Genetics (NASDAQ: FLGT) has announced it will release its third quarter 2024 financial results before the market opens on Friday, November 8, 2024. The company, which operates a laboratory services business and a therapeutic development business, will host a conference call for investors at 8:30 AM ET (5:30 AM PT) on the same day.
Management will discuss the results and answer questions during the call. Investors can access the live audio webcast through the Investor Relations section of Fulgent's website at http://ir.fulgentgenetics.com. An audio replay will also be available at the same location following the call.
Fulgent Genetics (NASDAQ: FLGT) reported Q2 2024 financial results with total revenue of $71.0 million. Core Revenue grew 5% year-over-year to $70.2 million. The company reported a GAAP loss of $8.7 million, or ($0.29) per share, and Non-GAAP income of $4.7 million, or $0.15 per share. Fulgent reiterated its Full Year 2024 Core Revenue Guidance of $280 million and improved its Earnings Per Share Guidance. The company maintains a strong cash position with $837.9 million in cash, cash equivalents, and investments as of June 30, 2024. Fulgent's Laboratory Services continue to show strength, particularly in Precision Diagnostics, while its Therapeutics Development segment progresses with clinical trials.
Fulgent Genetics (NASDAQ: FLGT) will announce its second quarter 2024 financial results on Friday, August 2, 2024, before the market opens.
The company will host a conference call for investors at 8:30 AM ET (5:30 AM PT) on the same day to discuss the results and answer questions.
The live audio webcast and replay will be accessible on Fulgent's Investor Relations website.
Fulgent Pharma, a subsidiary of Fulgent Genetics (NASDAQ: FLGT), presented Phase 1 clinical data on FID-007, its lead therapeutic oncology candidate, at the ASCO Annual Meeting on June 2, 2024. The study involved 11 patients with head and neck squamous cell carcinoma (HNSCC). Results showed a 45% partial response (PR) rate and a 27% stable disease (SD) rate. Three out of five patients with PR had previously been treated with taxane. The follow-up duration ranged from 1 to 15 months, and no high-grade neuropathy was observed. FID-007 demonstrated preliminary antitumor activity and lower toxicity. Fulgent has initiated a Phase 2 study of FID-007 in combination with cetuximab for HNSCC patients.
Fulgent Pharma, a subsidiary of Fulgent Genetics (NASDAQ: FLGT), announced the presentation of Phase 1 clinical data on its lead oncology candidate, FID-007, at the ASCO 2024 Annual Meeting. FID-007, a novel nanoparticle paclitaxel formulation, is being studied for the treatment of head and neck squamous cell carcinoma. The presentation will take place on June 2, 2024, in Chicago, Illinois, in a poster session during the Head and Neck Cancer track. Specific details include the abstract title, session, date, time, and poster board number.
Moffitt Cancer Center and Fulgent Pharma, a subsidiary of Fulgent Genetics (NASDAQ: FLGT), have announced a strategic partnership aimed at advancing cancer treatment. This collaboration combines Moffitt’s clinical capabilities with Fulgent’s nanotherapeutics and genomics platforms to accelerate the development of personalized cancer therapies.
Under the agreement, Moffitt will provide Fulgent with priority access to its clinical resources to expedite the advancement of Fulgent’s clinical pipeline. Fulgent's nanoencapsulation technology has already transformed paclitaxel into the soluble FID-007, showing substantial tumor reduction in Phase 1 studies.
The partnership will also co-develop next-generation personalized treatment options, leveraging Moffitt's scientific expertise and Fulgent's nano-particle-based drug development platform and genetic testing capabilities.
Brixton Biosciences has announced a successful Series B funding round, raising $33M. The funds will be used to advance their Neural Ice™ platform, a drug-free, injectable nerve block designed to provide long-lasting pain relief for 3-6 months. This funding will support pivotal clinical studies targeting knee pain from osteoarthritis and knee replacement surgery. The round was led by Schooner Capital, with participation from several other investors. The company also announced the appointment of Dr. Michael Fishman as Chief Medical Officer and industry veteran Reggie Groves to the Board of Directors. The Neural Ice™ platform has received Breakthrough Device Designation from the FDA, and early clinical results are promising.
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