Humanigen, Inc. is a biopharmaceutical company focused on preventing and treating certain inflammatory and oncological conditions. Humanigen, f/k/a KaloBios Pharmaceuticals and once led by the convicted Martin Shkreli, faced bankruptcy and reorganization after his arrest. By late 2019, it was struggling financially. However, when the COVID-19 pandemic emerged, Humanigen pivoted to explore its main drug, lenzilumab, originally developed for cancer, as a potential COVID-19 treatment. Pomerantz brought a securities class action against Humanigen for allegedly misrepresenting the effectiveness of lenzilumab for treating COVID-19 while failing to disclose important risks associated with the drug for patients with lung issues. The defendants did not inform investors that GM-CSF, which lenzilumab blocks, is crucial for lung health. After the FDA rejected lenzilumab’s Emergency Use Application on September 9, 2021, citing that the risks outweighed the benefits, executives continued to promote the drug’s prospects. The complaint further alleged that the news of the FDA rejection caused the stock price to plummet nearly 50%. After the results of a clinical trial were published, which failed to prove that lenzilumab was effective against COVID-19, the stock price dropped again, this time nearly 80%. Led by attorney Brenda Szydlo, Pomerantz recently secured a $3 million settlement for defrauded Humanigen investors. The firm is proud of this achievement; there is a need for transparency and corporate accountability in the biopharmaceutical industry, where public health and investor trust are on the line. #Biopharma #InvestorProtection #CorporateAccountability #TransparencyMatters #SecuritiesLitigation #ClassAction
Pomerantz LLP’s Post
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Biopharmaceutical companies that develop cancer treatments bring hope to millions of patients, and often profit handsomely along the way. However, while shareholders are eager for positive news about a company’s prospects, misrepresenting regulatory statements in the pharmaceutical industry—where lives are on the line—is exceedingly dangerous. Pomerantz recently achieved a $19.65 million settlement in a shareholder suit against Y-mAbs Therapeutics, Inc., a clinical biopharmaceutical company specializing in antibody-based therapies. According to the complaint, Y-mAbs misrepresented the FDA’s concerns about certain data in the company’s approval application for its neuroblastoma treatment, omburtamab, misleading investors into believing that omburtamab was on track for approval when in fact the FDA had identified serious issues with the data used as a control group in a study of the drug’s efficacy. When the FDA denied approval for omburtamab, the company's stock price sharply declined, resulting in significant losses for investors. #MedicalInnovation #PharmaceuticalIndustry #InstitutionalInvestors #SecuritiesLitigation #ClassAction
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Several days ago the UK health authority, MHRA, approved Amgen’s bone cancer drug Xgeva (denosumab) which is notable as the first drug submitted through the international recognition procedure (IRP). The IRP started this January and shortens applications to 60-110 days, instead of the current 150-days. The process includes regulators denoted as trusted. These streamlined regulatory authorization processes are part of a new accelerated approach of getting innovative therapies to patients faster. #biotechnology #pharmaceutical #riskmanagement #compliance
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Thoughts on this? >> Biotech Stocks Diverge On New Results For Weight-Loss Drug In MASH Patients - Investor's Business Daily >> Comment below! >>> lqventures.com #strategy #competitiveintelligence #marketing #biotech #pharma #pharmaceutical #healthcare #competitivemarketing
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Thoughts on this? >> Syndax's menin inhibitor succeeds in pivotal trial, but investors aren't impressed >> Comment below! >>> lqventures.com #strategy #competitiveintelligence #marketing #productmarketing #pharma #biotech #pharmaceutical #healthcare
Syndax's menin inhibitor succeeds in pivotal trial, but investors aren't impressed
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> CordenPharma Invests in End-to-End CDMO Supply Expansions across Six Technology Platforms, by Dr. Stephan Haitz: https://lnkd.in/en64tRe9 In PHARMAnetwork Magazine's Nov 2024 issue on CDMO Strategic Investment & Growth, discover how CordenPharma stays at the forefront of science by growing capacities in line with the expanding demand to provide bespoke end-to-end services that support pharma & biotech customers' complex modalities across the drug development spectrum. With our fully-integrated supply model as an overarching focus, CordenPharma has made significant investments across all six technology platforms (Peptides, Injectables, Lipids & Carbohydrates, Highly Potent & Oncology, Small Molecules, and Oligonucleotides). #CordenPharma #cdmo #integratedsupply #lipids #lnps #peptides #injectables #smallmolecules #osd #highlypotent #hpapis #oligos #pharmaceuticals #investment #glp1s #mrna #drugproducts
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Thoughts on this? >> Biotech Stocks Diverge On New Results For Weight-Loss Drug In MASH Patients - Investor's Business Daily >> Comment below! >>> lqventures.com #strategy #competitiveintelligence #marketing #pharma #competitivemarketing #healthcare #pharmaceutical #biotech
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Thoughts on this? >> Syndax's menin inhibitor succeeds in pivotal trial, but investors aren't impressed >> Comment below! >>> lqventures.com #strategy #competitiveintelligence #marketing #healthcare #pharma #productmarketing #pharmaceutical #biotech
Syndax's menin inhibitor succeeds in pivotal trial, but investors aren't impressed
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Biosimilars are more cost-effective treatment options than their reference products. By entering the market and competing with these reference products, biosimilars can drive down the prices of the originator biologics. This price reduction not only makes treatments more affordable but also increases accessibility, allowing a greater number of patients to receive essential medicines. Download the Report: https://bit.ly/47WvTBg #CancerCare #AffordableHealthcare #Biosimilars #HealthcareForAll #BioconBiologics #ClarivateReport
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#Announcement Trillioni Pharma achieves a new milestone! In line with our ongoing commitment to expanding pharmaceuticals to meet the diverse needs of our clients, we announce our strengthened presence in Germany through a new partnership with an EU GMP-certified manufacturer specialized in oncology products. With each new partnership, we enhance our role in streamlining communication between buyers and pharmaceutical manufacturers worldwide. Contact us for further inquiries and discuss your investment options. www.trillionipharma.com info@trillionipharma.com #Pharma #Trillioni #TrillioniPharma #TrillioniPlatform #TrillioniPharmaPlatform #PharmaceuticalManufacturing #Manufacturing #PharmaceuticalProducts #Medicine #Health #HealthCare #Germany #Partnership #GlobalNetWork #NewDeals #GMP #EU #Oncology #Oncological
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