Welcome to our dedicated page for Akero Therapeutics news (Ticker: AKRO), a resource for investors and traders seeking the latest updates and insights on Akero Therapeutics stock.
Akero Therapeutics, Inc. (Nasdaq: AKRO) is a clinical-stage biotechnology company based in South San Francisco, developing innovative treatments for major metabolic diseases, including non-alcoholic steatohepatitis (NASH). Focused on creating best-in-class medicines, Akero's lead clinical program centers on efruxifermin (EFX), a modified FGF21 protein designed to reduce liver fat, inflammation, and fibrosis. EFX is engineered to target both the liver and adipose tissue, offering potential comprehensive benefits to NASH patients.
Building on over two decades of FGF21 research, Akero has achieved significant milestones. Their Phase 2b HARMONY study, evaluating EFX in pre-cirrhotic NASH patients, demonstrated impressive results at Week 96, including substantial fibrosis improvement and liver health biomarkers. Additionally, the SYNCHRONY program encompasses multiple Phase 3 clinical trials aimed at both cirrhotic and pre-cirrhotic NASH patients, further validating the efficacy and safety profile of EFX.
Akero's rigorous clinical trials and outstanding engagement with the FDA underscore their commitment to addressing high unmet medical needs. Their recent public stock offering has bolstered financial stability, ensuring sustained progress in their groundbreaking research and development efforts. For more information, visit Akero Therapeutics and follow them on LinkedIn and Twitter.
Akero Therapeutics (Nasdaq: AKRO) announced upcoming presentations at the 75th Annual AASLD The Liver Meeting® 2024, showcasing data on efruxifermin (EFX) for treating pre-cirrhotic metabolic dysfunction-associated steatohepatitis (MASH). The presentations include:
1. An oral presentation on EFX's significant improvement of liver fibrosis at Week 96 in the HARMONY study.
2. A late-breaking poster on EFX's reduction of at-risk MASH and near-complete histological disease reversal at Week 96.
3. Another late-breaking poster on AI and digital-based pathology corroborating fibrosis reduction observed with EFX treatment.
All presentations will be given by Dr. Mazen Noureddin from Houston Methodist Hospital. The meeting takes place from November 15-19, 2024, in San Diego.
Akero Therapeutics (Nasdaq: AKRO), a clinical-stage company focused on developing treatments for serious metabolic diseases, has announced its participation in the H.C. Wainwright 8th Annual MASH Virtual Conference. The company's management will engage in a fireside chat on Monday, October 7, 2024, at 11:00 a.m. E.T.
Interested parties can access a live webcast of the presentation through the investor relations section of Akero's website at www.akerotx.com. For those unable to attend the live event, an archived replay will be made available on the company's website following the presentation.
Akero Therapeutics (Nasdaq: AKRO) has initiated dosing in the Phase 3 SYNCHRONY Outcomes trial, evaluating efruxifermin (EFX) for treating compensated cirrhosis due to metabolic dysfunction-associated steatohepatitis (MASH). This study is part of the broader SYNCHRONY Phase 3 program, which includes two other ongoing trials: SYNCHRONY Histology and SYNCHRONY Real-World. The program aims to assess EFX's efficacy in improving fibrosis, resolving MASH, and impacting long-term clinical outcomes across various stages of liver disease.
Key points:
- First patient dosed in SYNCHRONY Outcomes trial for compensated cirrhosis (F4) due to MASH
- SYNCHRONY program evaluates EFX in different stages of MASH severity
- Patients self-administer EFX using LyoJect 3S dual chamber syringe
- Week 96 results from Phase 2b SYMMETRY study expected in Q1 2025
Akero Therapeutics, Inc. (Nasdaq: AKRO), a clinical-stage company focused on developing treatments for serious metabolic diseases, has announced its participation in the Morgan Stanley 22nd Annual Global Healthcare Conference. The presentation is scheduled for Wednesday, September 4, 2024, at 7:45 a.m. E.T. in New York, NY.
Investors and interested parties can access a live webcast of the presentation through the investor relations section of Akero's website at www.akerotx.com. For those unable to attend the live event, an archived replay will be made available on the company's website following the presentation.
Akero Therapeutics (Nasdaq: AKRO) reported Q2 2024 financial results and provided business updates. Key highlights include:
1. Initiated Phase 3 SYNCHRONY Outcomes trial for efruxifermin (EFX) in patients with compensated cirrhosis due to MASH.
2. Presented promising 96-week data from Phase 2b HARMONY study at EASL Congress 2024, showing significant fibrosis improvement.
3. Appointed Scott Gangloff as Chief Technical Officer.
4. Cash position of $848.3 million as of June 30, 2024, expected to fund operations into second half of 2027.
5. R&D expenses increased to $55.3 million in Q2 2024, up from $28.0 million in Q2 2023.
6. Total operating expenses were $65.7 million in Q2 2024, compared to $35.6 million in Q2 2023.
Akero Therapeutics has initiated the SYNCHRONY Outcomes Phase 3 trial to evaluate efruxifermin (EFX) in patients with compensated cirrhosis (F4) due to MASH. This trial, which will enroll patients globally, aims to assess the efficacy and safety of EFX. The primary histology endpoint is fibrosis regression without worsening MASH after 96 weeks, and the primary outcomes endpoint is all-cause mortality and liver-related clinical outcomes.
The SYNCHRONY program includes three trials: Histology, Real-World, and Outcomes, each focused on different stages of MASH. EFX will be administered via the LyoJect 3S dual chamber syringe, a device designed for self-administration.
Akero Therapeutics has announced significant findings from the Phase 2b HARMONY study on efruxifermin (EFX) presented at the EASL Congress 2024. The 96-week data demonstrated that EFX achieved a ≥1-stage improvement in fibrosis without worsening metabolic dysfunction-associated steatohepatitis (MASH) in patients. At 96 weeks, 75% of patients on 50 mg EFX and 46% on 28 mg EFX showed improvement, compared to 24% for placebo. Additionally, 36% and 31% of patients on 50 mg and 28 mg EFX, respectively, exhibited a 2-stage improvement in fibrosis. The treatment was well tolerated, with no liver injury or decompensation events. A poster presentation highlighted EFX's positive impact on extracellular matrix remodeling and liver injury biomarkers, suggesting enhanced metabolic and liver health.
Akero Therapeutics (Nasdaq: AKRO), a clinical-stage company developing treatments for serious metabolic diseases, announced it will present at the Jefferies Global Healthcare Conference on June 5, 2024, at 4:00 p.m. ET in New York. The presentation will be available via live webcast on the company's investor relations webpage, with an archived replay accessible afterward.
Akero Therapeutics, Inc. (Nasdaq: AKRO) reported successful Week 96 results from the Phase 2b HARMONY study, showing significant improvements in fibrosis stage with the drug EFX in patients with pre-cirrhotic MASH. The company is well-funded with over $900 million in cash following an equity offering. Phase 3 SYNCHRONY studies are on track, including the SYNCHRONY Outcomes study for patients with cirrhosis. Akero also closed a public offering of common stock, raising approximately $366.9 million. Financially, the company has $903.7 million in cash and saw increased expenses related to clinical studies and operations.
Akero Therapeutics, a clinical-stage company focused on treatments for metabolic diseases, will present at the BofA Securities 2024 Health Care Conference on May 14, 2024, in Las Vegas, NV. The presentation can be accessed through the company's website.
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