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STOCK RECAP #PipelineProspector

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Pipeline Prospector Nov 2024: Trump’s HHS pick drags down jab makers’ stocks; Novartis, Merck, Roche ink billion-dollar deals
In November, the markets responded to US President-elect Donald Trump’s picks, particularly the choice of Robert F. Kennedy Jr. to lead the Department of Health and Human Services (HHS). Given that RFK Jr. is known as an anti-vaccine activist, stocks of Pfizer, Novavax, and Moderna dipped by 10 percent, 10 percent and 20 percent respectively during the month. Vaccine makers in Europe, such as GSK and Bavarian Nordic, also met a similar fate, and their stocks were down by 11 percent and 9 percent respectively for the month.Overall, the Nasdaq Biotechnology Index (NBI) fell by 0.11 percent — from 4,650.07 to 4,644.81 in November. The SPDR S&P Biotech ETF (XBI) rebounded 2.67 percent from 97.03 to 99.62, while the S&P Biotechnology Select Industry Index (SPSIBI) ended higher by 2.68 percent — from 7,561.3 to 7,763.7. Access the Pipeline Prospector Dashboard for November 2024 Newsmakers (Free Excel)Pharma giants Novartis, Merck, Roche spark November’s billion-dollar deal bonanzaSwiss drugmakers — Novartis and Roche — dominated this month’s dealmaking landscape. Novartis acquired Kate Therapeutics for up to US$ 1.1 billion, targeting Duchenne muscular dystrophy and other neuromuscular diseases.Novartis also committed US$ 150 million upfront to computational drug discovery firm Schrödinger (stock up 21 percent) in a research collaboration and license deal that has the potential to reach US$ 2.45 billion.In yet another deal, Novartis committed US$ 745 million to Ratio Therapeutics for a radiotherapeutic candidate being developed to cure cancer. The company CEO Vas Narasimhan plans to keep pursuing strategic acquisitions under US$ 5 billion. Over the last five years, the company has spent approximately US$ 19.4 billion in deals.Roche entered into a US$ 1.8 billion deal with Flare Therapeutics to target previously undrugged cancer transcription factors (i.e. proteins that regulate the transcription of genes). It also acquired Poseida Therapeutics for up to US$ 1.5 billion. The acquisition of Poseida (stock up 350 percent) brings innovative CAR-T programs for solid tumors and autoimmune diseases within its fold.American drugmaker Sarepta Therapeutics (stock up 9 percent) signed a landmark deal with Arrowhead Pharmaceuticals (stock up 35 percent), valued at up to US$ 11.4 billion. It includes an  upfront payment of US$ 500 million, an equity investment of US$ 325 million, and worldwide rights to seven RNA-based programs (four clinical, three preclinical). Milestone payments and royalties make up for US$ 10 billion. The collaboration “affords multiple potential blockbuster opportunities” across skeletal muscle, cardiac, and central nervous system disorders.BioNTech (stock up 5 percent) is buying Chinese biotech firm Biotheus for up to US$ 950 million. And Merck signed a US$ 3.3 billion deal with China’s LaNova Medicines for LM-299, a bispecific antibody. Both these deals manifest growing interest in PD-(L)1xVEGF bispecific antibodies, intended for treating solid tumors. Access the Pipeline Prospector Dashboard for November 2024 Newsmakers (Free Excel) Journey Medical, UCB secure FDA nods for skin treatments; BridgeBio’s Attruby to take on Pfizer’s VyndaqelBridgeBio Pharma (stock up 8 percent) made an "improbable comeback" after a disastrous trial failure and two rounds of layoffs. It clinched FDA’s nod for Attruby, the first new treatment for transthyretin amyloid cardiomyopathy (a rare heart disease) in over five years. With this potentially transforming treatment option, BridgeBio gains a foothold in a lucrative market dominated by Pfizer’s blockbuster Vyndaqel. Attruby is expected to bring in US$ 2.5 billion in peak sales by 2035.In dermatology, Journey Medical secured approval for Emrosi, an innovative oral antibiotic developed along with Dr. Reddy’s Laboratories for treating rosacea (an inflammatory skin condition). UCB’s Bimzelx received its fifth FDA approval in just over a year, becoming the first therapy to selectively inhibit two proteins —  IL-17A and IL-17F — to treat hidradenitis suppurativa, a painful skin condition. And Johnson & Johnson’s oral drug icotrokinra achieved successful phase 3 results in moderate-to-severe plaque psoriasis (a skin condition where inflamed and scaly plaques appear on the skin).In oncology and hematology, Syndax Pharmaceuticals’ Revuforj became the first menin inhibitor approved for relapsed or refractory acute leukemia. And Azurity Pharmaceuticals bagged an FDA nod for Danziten (nilotinib), a formulation of Novartis’ blockbuster drug Tasigna that allows patients with chronic myeloid leukemia (a blood cancer that begins with the bone marrow) to take their medication without fasting.Autolus Therapeutics achieved its first FDA approval. Its med Aucatzyl for relapsed or refractory B-cell precursor acute lymphoblastic leukemia became the first FDA-approved CAR-T therapy without the agency’s drug safety program requirement, known as Risk Evaluation and Mitigation Strategies (REMS). Its REMS-free status could simplify its administration and increase its adoption among treatment centers.Other significant nods include PTC Therapeutics’ Kebilidi – the first-ever FDA approval for a gene therapy directly administered to the brain and, Jazz Pharmaceuticals’ Ziihera for HER2-positive biliary tract cancer. Access the Pipeline Prospector Dashboard for November 2024 Newsmakers (Free Excel) Novo, AbbVie, Cassava face trial failures; FDA rejects Lexicon, Applied Therapeutics’ drugsThe US Food and Drug Administration’s advisory committee rejected Lexicon Pharmaceuticals’ diabetes drug Zynquista, citing diabetic ketoacidosis risks for type 1 diabetes patients with chronic kidney disease. In 2023, the drug had been approved for heart failure.Applied Therapeutics saw the FDA reject its galactosemia drug, govorestat, dampening hopes for its first commercial product. Cassava Sciences’ Alzheimer’s drug simufilam, once hailed as a potential breakthrough, missed pivotal trial endpoints amid ongoing fraud investigations involving neuroscientist Hoau-Yan Wang. Critics questioned the validity of the preclinical and early clinical data, suggesting that the promising results may have been overstated or fabricated.Lexicon, Cassava, and Applied Therapeutics’ stocks plummeted 40 percent, 85 percent, and 78 percent, respectively.AbbVie (stock down 10 percent) faced a significant blow as emraclidine, the centerpiece of its US$ 8.7 billion Cerevel acquisition, failed to meet primary endpoints in two pivotal phase 2 schizophrenia trials.Novo Nordisk (stock down 5 percent) decided to discontinue kidney disease drug ocedurenone after a phase 3 trial failure, resulting in an impairment loss of approximately US$ 816.5 million. Access the Pipeline Prospector Dashboard for November 2024 Newsmakers (Free Excel) Our viewIn the third quarter of 2024, Pfizer recorded a 32 percent increase in its year-on-year sales, ending a six-quarter streak where either Eli Lilly or Novo Nordisk were leading in revenue growth. Despite this feat, Pfizer’s stock took a beating on the bourses due to RFK Jr’s nomination to head the HHS.Trump has nominated another controversial personality — Johns Hopkins’ surgeon Martin Makary — to head the FDA. Makary has been a critic of Covid-19 mandates such as masking and vaccines. While the markets didn’t react to his nomination, going forward, we foresee political headwinds causing some turbulence in the biopharma industry. Access the Pipeline Prospector Dashboard for November 2024 Newsmakers (Free Excel) 

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https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-nov-2024-trump-s-hhs-pick-drags-down-jab-makers-stocks-novartis-merck-roche-ink-billion-dollar-deals

#PharmaFlow by PHARMACOMPASS
05 Dec 2024

WEEKLY NEWS RECAP #Phispers

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Novartis snaps up PTC’s Huntington’s disease program in US$ 2.9 bn deal; Sanofi to set up insulin facility in China
In Phispers this week, we bring you news of how political changes in the US could impact the pharma industry. Big Pharma has reportedly begun lobbying with Trump for an ease in Medicare price negotiations put in place by the Biden-Harris administration. And the former chief of the US Food and Drug Administration (FDA) Scott Gottlieb has raised serious concerns over the nomination of Robert F. Kennedy Jr as the Secretary of the Health and Human Services (HHS).After forging three deals last month, Novartis has signed a US$ 2.9 billion deal this week with PTC Therapeutics to license its Huntington’s disease program. Takeda has partnered Keros Therapeutics, promising it up to US$ 1.3 billion for a candidate that targets anemia in hematologic cancers.GSK has entered into a deal with Chinese biotech Duality Biologics to obtain a license to develop and commercialize its preclinical molecule that targets gastrointestinal (GI) cancer. Sanofi has announced its largest investment in China by committing US$ 1.05 billion to set up a new insulin facility in Beijing. And Roche’s Genentech has entered into a potential US$ 940 million deal with COUR Pharmaceuticals to address an undisclosed autoimmune disease.In drug approvals, FDA has okayed AstraZeneca’s blockbuster drug Imfinzi to treat adults with limited-stage small cell lung cancer. The agency has also approved Merus’ Bizengri for hard to treat cancers.And, after rejecting its drug last week, FDA has issued a warning letter to Applied Therapeutics for deleting critical electronic data, and for making a dosing mistake in its clinical trial.Novartis licenses PTC’s Huntington’s disease program for up to US$ 2.9 bnNovartis is paying US$ 1 billion upfront to PTC Therapeutics and an additional US$ 1.9 billion for its PTC518 Huntington’s disease program. PTC518 is an innovative oral therapy designed to reduce the production of the mutant huntingtin protein, the root cause of Huntington’s disease. PTC said the deal was signed after “a highly competitive process with several parties involved.” Additionally, PTC will be entitled to a 40 percent share of US profits.Takeda in potential US$ 1.3 bn deal with Keros: Takeda has licensed Keros Therapeutics’ elritercept, a late-stage activin inhibitor designed to treat anemia associated with hematologic cancers such as myelodysplastic syndromes (MDS) and myelofibrosis (MF). The deal includes a US$ 200 million upfront payment to Keros, with potential milestone payments that could exceed US$ 1.1 billion. Elritercept has shown promising results in early clinical trials, demonstrating significant reductions in transfusion dependence and improvements in anemia symptoms for patients with MDS and MF.Big Pharma lobbying Trump to ease Medicare price negotiations, says ReutersThe US pharmaceutical industry is lobbying the incoming Trump administration to revise the Inflation Reduction Act (IRA), which allows Medicare to negotiate prices for its costliest prescription drugs. Industry executives and lobbyists told Reuters, Big Pharma is pushing to delay the timeline for when medications become eligible for price negotiations by four years for small molecule drugs, which are primarily pills.According to analysts at S&P Global, Trump has “significant ability to potentially influence US healthcare”. They have highlighted several areas of concern, including developments related to the Affordable Care Act and the fact that Trump has threatened to roll back parts of the IRA.Gottlieb raises concerns over RFK Jr’s nomination to head HHS: Scott Gottlieb, an industry-favored FDA commissioner who served during Trump’s first term, has raised serious concerns about President-elect Donald Trump’s nomination of Robert F. Kennedy Jr. as Secretary of HHS. Gottlieb warned that Kennedy’s long-standing vaccine skepticism could lead to a significant decline in vaccination rates for diseases like measles, mumps, and rubella, potentially resulting in large outbreaks and preventable deaths. “I think if RFK follows through on his intentions, and I believe he will, and I believe he can, it will cost lives in this country,” said Gottlieb.FDA okays Astra’s Imfinzi for limited stage small cell lung cancerFDA has okayed AstraZeneca’s blockbuster drug Imfinzi (durvalumab) to treat adults with limited-stage small cell lung cancer whose disease has not progressed following concurrent platinum-based chemotherapy and radiation therapy. Imfinzi is a human monoclonal antibody and an alternative to chemotherapy. It blocks a tumor’s ability to evade and dampen the immune system, and boosts the body’s anti-cancer immune response.Merus’ therapy okayed: FDA has approved Merus NV’s therapy — Bizengri — that targets the NRG1 gene. The gene is associated with the formation and progression of several tumors. Bizengri (zenocutuzumab-zbco) is the first and only treatment indicated for adults with pancreatic adenocarcinoma or non–small cell lung cancer that are advanced, unresectable or metastatic and harbor NRG1 gene fusion. These cancers are hard to treat.Sanofi announces US$ 1 bn investment in China for new insulin production facilitySanofi has announced its largest investment in China, committing € 1 billion (US$ 1.05 billion) to establish a new insulin production facility in the Beijing Economic and Technological Development Zone. This new site will be Sanofi’s fourth production facility in China and is designed to enhance local end-to-end insulin production capabilities.GSK inks deal with DualityBio: Shanghai-headquartered clinical-stage biotech Duality Biologics has entered into an exclusive option agreement with GSK for its antibody-drug conjugate (ADC) candidate, DB-1324. Under the agreement, DualityBio will grant GSK an exclusive option to obtain a license to develop and commercialize DB-1324 worldwide (excluding mainland China, Hong Kong, and Macau). DB-1324 is a molecule in preclinical development that targets gastrointestinal (GI) cancer.Genentech-COUR in autoimmune deal: Roche’s Genentech has entered into a strategic collaboration with COUR Pharmaceuticals to develop and commercialize the latter’s proprietary tolerogenic nanoparticle treatments for an undisclosed autoimmune disease. The deal includes US$ 40 million in upfront payments, with the potential of milestone payments that could exceed US$ 900 million.After rejecting drug, FDA issues warning letter to Applied TherapeuticsApplied Therapeutics has received a warning letter from the FDA regarding its clinical trial for the genetic disease drug, govorestat. The FDA cited issues with the company’s trial conduct, including the deletion of critical electronic data, which compromised the integrity of the study. The letter highlighted a dosing mistake where at least 19 patients were given a lower dose of the drug than what was specified in the protocol. This warning comes shortly after the FDA declined to approve govorestat for treating galactosemia, a rare metabolic disorder where galactose found in milk builds up in tissues and blood.  

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https://www.pharmacompass.com/radio-compass-phisper/novartis-snaps-up-ptc-s-huntington-s-disease-program-in-us-2-9-bn-deal-sanofi-to-set-up-insulin-facility-in-china

#Phispers by PHARMACOMPASS
05 Dec 2024

NEWS #PharmaBuzz

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https://www.globenewswire.com/news-release/2025/12/11/3204367/0/en/Cycle-Pharmaceuticals-to-Acquire-Applied-Therapeutics.html

GLOBENEWSWIRE
12 Dec 2025

https://www.fiercebiotech.com/biotech/analysts-question-if-applied-tx-can-ever-get-rare-disease-drug-market-fda-talks-drag

FIERCE BIOTECH
14 Nov 2025

https://www.globenewswire.com/news-release/2025/11/13/3187173/0/en/Applied-Therapeutics-Reports-Third-Quarter-2025-Financial-Results.html

GLOBENEWSWIRE
13 Nov 2025

https://www.globenewswire.com/news-release/2025/09/29/3157573/0/en/Applied-Therapeutics-Provides-Update-Following-Meeting-with-FDA.html

GLOBENEWSWIRE
29 Sep 2025

https://www.globenewswire.com/news-release/2025/05/18/3083535/0/en/Applied-Therapeutics-Presents-Full-12-Month-Clinical-Results-and-New-Topline-Data-from-INSPIRE-Phase-2-3-Trial-of-Govorestat-in-CMT-SORD-in-Late-Breaking-Oral-Presentation-at-the-P.html

GLOBENEWSWIRE
18 May 2025

https://www.globenewswire.com/news-release/2024/05/09/2878591/0/en/Applied-Therapeutics-Reports-First-Quarter-2024-Financial-Results.html

GLOBENEWSWIRE
09 May 2024