Welcome to our dedicated page for Ironwood news (Ticker: IRWD), a resource for investors and traders seeking the latest updates and insights on Ironwood stock.
Ironwood Pharmaceuticals, Inc. (NASDAQ: IRWD) is a biopharmaceutical company dedicated to creating innovative medicines that significantly improve the lives of patients. Founded in 1998, Ironwood specializes in gastrointestinal (GI) therapeutics and has a strong focus on developing and commercializing treatments for chronic conditions of the GI tract.
The company's flagship product is a medicine designed for adults suffering from irritable bowel syndrome with constipation (IBS-C) and chronic idiopathic constipation (CIC). This medicine, discovered and developed by Ironwood, is now fully commercialized and widely used to alleviate symptoms in patients, improving their quality of life.
Ironwood's research pipeline is robust, with multiple investigational medicines targeting both the upper and lower GI tract. The company leverages its expertise in gastrointestinal disorders and pharmacologic expertise in guanylate cyclases to develop new therapies that address unmet medical needs.
Beyond its core product, Ironwood is actively exploring new opportunities and expanding its portfolio through collaborative licenses, commercial agreements, and strategic acquisitions. These efforts aim to enhance the company's research, development, manufacturing, and marketing capabilities, thereby driving growth and innovation.
Recent achievements for Ironwood include the advancement of several clinical trials, promising data from ongoing research studies, and strategic partnerships aimed at enhancing product development and market reach. Financially, Ironwood continues to build value, achieving milestones that attract continued support from shareholders.
Ironwood Pharmaceuticals remains committed to its mission of making a difference for patients through the development of groundbreaking therapies. The company’s strong pipeline, dedicated team, and strategic initiatives position it as a leading player in the field of gastrointestinal therapeutics.
Ironwood Pharmaceuticals (NASDAQ: IRWD) will participate in two upcoming virtual investor conferences in September 2021. The Wells Fargo Healthcare Conference is scheduled for September 10 at 2:00 p.m. ET, and the Morgan Stanley 19th Annual Global Healthcare Conference will take place on September 13 at 2:45 p.m. ET. Investors can access live webcasts on Ironwood's website, with replays available for 14 days post-conference. Ironwood focuses on developing medicines for gastrointestinal diseases, notably linaclotide for IBS-C and CIC.
Ironwood Pharmaceuticals (NASDAQ: IRWD) announced FDA approval for a revised label of LINZESS (linaclotide) based on pediatric clinical safety data. The update narrows the boxed warning for dehydration risks to children under two years, previously applicable to all under 18. The labeling reflects ongoing studies to enhance safety profiles for pediatric use. LINZESS remains contraindicated for children under two, and its effectiveness for patients under 18 is not yet established. The drug is indicated for adults with irritable bowel syndrome with constipation (IBS-C) and chronic idiopathic constipation (CIC).
Ironwood Pharmaceuticals (Nasdaq: IRWD) reported robust Q2 2021 financial results, achieving total revenues of $104 million, a 16% increase from Q2 2020. GAAP net income surged to $391 million, or $2.42 per share, compared to $25 million, or $0.16 per share, in the prior year. LINZESS, its primary product, saw an 18% rise in U.S. net sales to $259 million. Ironwood raised its 2021 guidance, expecting total revenue of $390 to $410 million, driven by increasing demand for LINZESS. The company also highlighted promising developments in its pipeline, including IW-3300, targeting visceral pain conditions.
Ironwood Pharmaceuticals (NASDAQ: IRWD) has appointed John Minardo as senior vice president and chief legal officer. He will serve on the Leadership Team, overseeing the Corporate Legal, Compliance, and IP teams, and report to CEO Thomas McCourt. Minardo brings over 20 years of legal experience in healthcare, previously serving in key legal roles at Seqirus and Novartis. His appointment is expected to enhance Ironwood's strategy and focus on improving treatments for gastrointestinal diseases.
Ironwood Pharmaceuticals (NASDAQ: IRWD) will host its second quarter 2021 investor update conference call on August 5, 2021, at 8:30 a.m. ET. Participants can join by dialing (833) 350-1432 (U.S. and Canada) or (647) 689-6932 (international) using conference ID 2598317. A replay will be available from 11:30 a.m. ET the same day until 11:59 p.m. ET on August 19, 2021. Ironwood specializes in GI diseases and is known for its leadership in linaclotide for treating IBS-C and CIC.
Ironwood Pharmaceuticals (NASDAQ: IRWD) announced the publication of Phase IIIb trial results for LINZESS (linaclotide) in the American Journal of Gastroenterology. The study demonstrated that 290 mcg of linaclotide significantly improved abdominal symptoms among adults with irritable bowel syndrome with constipation (IBS-C). Results showed a 29.7% decrease in abdominal scores compared to an 18.3% decrease with placebo, starting from week one. LINZESS was well-tolerated, with diarrhea being the most common adverse effect. The findings aim to enhance patient-doctor communication concerning IBS-C symptoms.
Ironwood Pharmaceuticals (NASDAQ: IRWD) has appointed Thomas McCourt as permanent CEO, having served as interim CEO since March 2021. His leadership aims to drive growth for LINZESS (linaclotide), a leading treatment for gastrointestinal conditions. Additionally, Gina Consylman will step down as CFO effective July 2, 2021, without any reported disagreements. The board commended her contributions, particularly during Ironwood's strategic transactions. McCourt expressed confidence in the company's financial stability and its future opportunities in the GI healthcare sector.
Ironwood Pharmaceuticals (NASDAQ: IRWD) announced an agreement with Teva Pharmaceuticals to license a generic version of LINZESS (linaclotide), allowing marketing to begin on March 31, 2029, pending FDA approval. This agreement settles all known ANDA filings for generic LINZESS. The patent coverage for LINZESS is preserved across three dosage strengths, reaffirming the company's plans to grow its franchise. The settlement will be submitted for review to regulatory authorities.
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