Welcome to our dedicated page for Chromadex news (Ticker: CDXC), a resource for investors and traders seeking the latest updates and insights on Chromadex stock.
ChromaDex Corp. (NASDAQ: CDXC), transitioning to the name Niagen Bioscience, Inc. with a new Nasdaq ticker symbol NAGE, generates a steady flow of news centered on NAD+ science and healthy aging. As the self-described global authority on nicotinamide adenine dinucleotide (NAD+), the company regularly issues updates on its Niagen ingredient, Tru Niagen supplement brand, and pharmaceutical-grade Niagen IV and injection products.
News for CDXC often includes financial results and outlooks, where ChromaDex reports quarterly and annual net sales, gross margins, net income, and cash flow metrics, along with commentary on trends in Tru Niagen and Niagen ingredient sales. These releases may also discuss expectations for future revenue growth, margin performance, and planned investments in research, development, and marketing.
Investors can also expect corporate and investor relations announcements, such as participation in healthcare and growth company conferences, investor summits, and panel discussions on longevity and supplementation. These events typically feature company management presenting ChromaDex’s strategy, financial performance, and updates on its NAD+ research and product pipeline.
Another key category of news involves product and partnership developments. ChromaDex has announced the expansion of Niagen IV and related pharmaceutical-grade Niagen products across wellness clinic networks, as well as collaborations where Niagen serves as a hero ingredient in third‑party longevity supplements. The company also highlights recognition in industry lists and awards related to health products and business impact.
Finally, ChromaDex issues scientific and regulatory updates, including information about FDA designations for nicotinamide riboside in rare disease indications and progress toward regulatory milestones. For anyone tracking CDXC, or its successor symbol NAGE, this news feed offers a consolidated view of the company’s financial performance, clinical and regulatory progress, commercial expansion, and branding evolution around Niagen and NAD+ science.
ChromaDex Corp. (NASDAQ:CDXC), a leader in NAD+ research and healthy aging, announces its participation in Canaccord Genuity's 44th Annual Growth Conference from August 13-15, 2024, in Boston. CEO Rob Fried and Interim CFO James Lee will present on August 14 and conduct one-on-one meetings throughout the event.
This prestigious conference, a 44-year cornerstone for industry leaders and investors, provides ChromaDex an opportunity to showcase its latest developments, strategic initiatives, and growth prospects. Interested parties can arrange meetings through the conference website or their CG representative.
ChromaDex's involvement underscores its commitment to engaging with investors and industry experts, potentially impacting its market position and future growth strategies in the healthy aging sector.
ChromaDex Corp. (NASDAQ:CDXC), a leader in NAD+ research and healthy aging, has announced its Q2 2024 financial results conference call. The call is scheduled for Wednesday, August 7, 2024, at 4:30 p.m. ET. Financial results will be released via press release after market close on the same day. Investors can join the call using the toll-free number 1-888-596-4144 (Conference ID: 8584242) or via webcast. Management will discuss Q2 results and provide a general business update. A replay will be available until August 14, 2024. This event offers investors an opportunity to gain insights into ChromaDex's financial performance and future outlook.
ChromaDex Corp. (NASDAQ:CDXC) has launched the Niagen+ NAD+ Test Kit, exclusively available through its healthcare practitioner (HCP) channel. This innovative kit allows practitioners to measure patient blood NAD+ levels, enabling more personalized protocols using ChromaDex's NAD+-boosting products, Tru Niagen® and Niagen+.
The test kit features advanced dried blood spot (DBS) assay technology, ensuring NAD+ sample stability during transport. Analysis is conducted using high-resolution liquid chromatography/tandem mass spectrometry (LC-MS/MS) at a CLIA and CAP accredited laboratory. Results are available to both patients and doctors in about two weeks through the 1health platform.
This launch represents a significant advancement in NAD+ therapy, allowing practitioners to track NAD+ changes over time and create more effective patient protocols.
ChromaDex Corp. (NASDAQ:CDXC) has appointed Carlos Lopez as Senior Vice President, General Counsel, effective July 22, 2024. Lopez, a distinguished legal professional with expertise in the dietary supplements industry, will oversee the organization's legal function, including corporate governance, securities, intellectual property, and litigation. He will report directly to CEO Rob Fried.
Prior to joining ChromaDex, Lopez served as Vice President, General Counsel at The Vitamin Shoppe and has been on the board of The Natural Products Association. CEO Rob Fried expressed confidence in Lopez's expertise to help achieve ChromaDex's ambitious plans. Lopez stated his excitement to join ChromaDex, recognizing it as the gold-standard company pioneering NAD+ research and innovation.
ChromaDex Corp. (NASDAQ:CDXC) announces the debut of pharmaceutical-grade Niagen® (nicotinamide riboside chloride) for intravenous and injectable use at leading wellness clinics in August. Wells Pharma of Houston, a U.S. FDA-registered 503B outsourcing facility, will compound and distribute Niagen+ to select IV clinics.
Niagen IV offers superior tolerability, a 75% shorter infusion time, and a higher, faster rise in NAD+ blood levels compared to standard NAD+ IV treatments. With the global intravenous hydration therapy market valued at over $2.32 billion in 2022, ChromaDex is well-positioned to capture a significant share with its new product.
The company has secured orders beyond August and plans to expand into medical spas, with 11,000 locations in the US alone. Several prominent wellness clinics, including Clean Market/NutriDrip, Next Health, REVIV, and Restore Hyper Wellness, have expressed enthusiasm for the launch of Niagen+.
ChromaDex announced its inclusion in the Russell 2000® Index, effective July 1, 2024, as part of the annual Russell indexes reconstitution. This milestone, highlighted by CEO Rob Fried, marks ChromaDex's sustained growth and leadership in NAD+ research. ChromaDex's flagship product, Tru Niagen®, is renowned for its scientific rigor and quality standards, offering a clinically proven NAD+ supplement to combat age-related health decline. The Russell 2000 Index includes the 4,000 largest U.S. stocks, and ChromaDex's inclusion reflects its robust market capitalization and potential to drive long-term shareholder value.
ChromaDex Corp. (NASDAQ:CDXC) announced promising results from a Phase II clinical study on their patented nicotinamide riboside (NR) ingredient, Niagen®. Conducted with Northwestern University Feinberg School of Medicine, the study revealed significant improvements in functional mobility for individuals with peripheral artery disease (PAD). Participants showed increased six-minute walking distance and treadmill walking time, compared to a placebo. These findings, now published in Nature Communications, indicate the potential of NR to benefit PAD patients. However, further confirmation through larger clinical trials is necessary.
ChromaDex is set to launch Niagen+, the first pharmaceutical-grade intravenous and injectable Niagen (Nicotinamide Riboside Chloride or NRC).
FDA-approved for compounding by 503B outsourcing facilities, Niagen+ IV and injectable forms will be available at clinics nationwide starting August 2024. A clinical study showed no adverse side effects, superior tolerability, and a faster infusion time compared to NAD+ IV, with blood NAD+ levels peaking higher and sooner.
Niagen+ aims to transform the $2.32 billion global intravenous hydration therapy market. ChromaDex holds over 80 patents for its NAD+ precursors, ensuring robust IP protection.
ChromaDex (NASDAQ: CDXC) has received Orphan Drug Designation (ODD) and Rare Pediatric Disease (RPD) Designation from the FDA for its product candidate Nicotinamide Riboside Chloride (NRC), aimed at treating Ataxia Telangiectasia (AT), a rare and life-threatening condition affecting children. The company intends to submit an Investigational New Drug (IND) application to the FDA to commence human clinical trials. These trials will be led by Dr. Vilhelm Bohr, a scientific advisor to ChromaDex. The designations could accelerate NRC's development and provide benefits like market exclusivity and tax credits. CEO Rob Fried highlighted the potential of NRC to address unmet medical needs in rare diseases, which affect over 30 million people in the U.S.
ChromaDex (NASDAQ: CDXC) will participate in Renmark Financial Communications Inc.'s Virtual Non-Deal Roadshow on June 11, 2024, at 2:00pm PST. The event will feature presentations from CEO Rob Fried and CFO Brianna Gerber, who will discuss the latest investor presentation and participate in a live Q&A session. Stakeholders and investors are encouraged to register for the live event, though access may be A replay will be available on the ChromaDex Investor Relations website. For further details, visit www.chromadex.com.
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