We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
Biotech Stock Roundup: Regulatory Updates From REGN, INCY, & Other Updates
Read MoreHide Full Article
The biotech sector continues to be in focus with regulatory and pipeline updates from quite a few companies. New drug approvals are also in the spotlight. The sector has also been in focus, thanks to the development of antibodies and vaccines for coronavirus gaining importance with each passing day.
Recap of the Week’s Most Important Stories:
Regeneron Obtains FDA Nod for Libtayo in NSCLC: RegeneronPharmaceuticals, Inc. (REGN - Free Report) and partner Sanofi (SNY - Free Report) obtained FDA approval for a label expansion of their PD-1 inhibitor, Libtayo (cemiplimab-rwlc). The drug is now approved for the first-line treatment of patients with advanced non-small-cell lung cancer (NSCLC) whose tumors have high PD-L1 expression (tumor proportion score ≥50%), as determined by an FDA-approved test. Libtayo was superior in extending overall survival compared to chemotherapy in a pivotal trial that allowed for certain disease characteristics frequently underrepresented in advanced NSCLC trials. Earlier this month, the drug was approved as the first immunotherapy for patients with advanced basal cell carcinoma (BCC) previously treated with a hedgehog pathway inhibitor (HHI) or for whom an HHI is not appropriate, with full approval granted for locally advanced disease and accelerated approval granted for metastatic disease.
Regulatory Updates From Incyte: Incyte (INCY - Free Report) announced that the FDA has accepted for Priority Review its supplemental New Drug Application (sNDA) for lead drug, Jakafi (ruxolitinib), for the treatment of steroid-refractory chronic graft-versus-host disease (GVHD) in adult and pediatric patients 12 years and older. The agency generally grants Priority Review to drugs that offer a major advancement in treatment where none currently exists. This designation shortens the review period to six months compared to 10 months for Standard Review. The target action date for this indication is Jun 22, 2021.
Separately, the agency has also accepted for Priority Review the New Drug Application (NDA) for ruxolitinib cream, a selective JAK1/JAK2 inhibitor designed for topical application, as a treatment for atopic dermatitis (AD), a type of eczema.
Nektar Up on Agreement With Merck: Shares of Nektar Therapeutics (NKTR - Free Report) gained after it announced an agreement with pharma giant Merck (MRK - Free Report) for a phase II/III study of the former’s bempegaldesleukin (NKTR-214, BEMPEG) in combination with the latter’s blockbuster immuno-oncology drug, Keytruda, for the first-line treatment of patients with metastatic or unresectable recurrent squamous cell carcinoma of the head and neck (SCCHN), whose tumors express PD-L1. Per the terms, Nektar will conduct the above-mentioned study, which is expected to enroll 500 patients with metastatic or recurrent SCCHN with PD-L1 expressing tumors. The company will conduct the above-mentioned study, which is expected to enroll 500 patients with metastatic or recurrent SCCHN with PD-L1 expressing tumors.
These patients will be randomized to receive either the combination of bempegaldesleukin and Keytruda or only Keytruda. The phase II portion of the study will include an interim analysis of the overall response rate (ORR) after the first 200 patients enrolled have a minimum follow-up of 4 months. The study will be continued only if the ORR passes a prespecified futility boundary.
Immunome Surges on Antibodies Update: Shares of Immunome, Inc. (IMNM - Free Report) surged after it announced that its discovery engine has isolated potent antibodies capable of neutralizing several SARS-CoV-2 variants, including the South African Variant (B.1.351), in pseudovirus testing. The company is developing a cocktail of antibodies targeting spike and non-spike proteins that can serve as a prophylaxis or treatment for COVID-19. Immunome has identified antibodies that bind to non-overlapping regions of the spike protein, including those regions containing the critical mutational variants while developing the antibody cocktail (IMM-BCP-001).
Otonomy Plunges on Study Data: Shares of Otonomy, Inc. plunged significantly after it announced that the late-stage study of Otividex was not successful. The phase III study of Otividex in patients with Ménière’s disease did not achieve the primary endpoint, which was the count of definitive vertigo days (DVD) in month 3 for Otividex as compared to placebo for the intent-to-treat (ITT) population (n = 148; p value = 0.312) using the Negative Binomial Model. The results did show statistical significance for the per protocol (PP) population.
Performance
Medical - Biomedical and Genetics Industry 5YR % Return
The Nasdaq Biotechnology Index lost 4.20% in the last five trading sessions. Among the biotech giants, Vertex gained 2.93% during the period. Over the past six months, shares of Alexion have surged 49.3%. (See the last biotech stock roundup here: Biotech Stock Roundup: REGN’s Drug Approval & Pipeline Updates From AMGN, BLUE)
What's Next in Biotech?
Stay tuned for more pipeline and regulatory updates.
Biggest Tech Breakthrough in a Generation
Be among the early investors in the new type of device that experts say could impact society as much as the discovery of electricity. Current technology will soon be outdated and replaced by these new devices. In the process, it’s expected to create 22 million jobs and generate $12.3 trillion in activity.
A select few stocks could skyrocket the most as rollout accelerates for this new tech. Early investors could see gains similar to buying Microsoft in the 1990s. Zacks’ just-released special report reveals 8 stocks to watch. The report is only available for a limited time.
Image: Bigstock
Biotech Stock Roundup: Regulatory Updates From REGN, INCY, & Other Updates
The biotech sector continues to be in focus with regulatory and pipeline updates from quite a few companies. New drug approvals are also in the spotlight. The sector has also been in focus, thanks to the development of antibodies and vaccines for coronavirus gaining importance with each passing day.
Recap of the Week’s Most Important Stories:
Regeneron Obtains FDA Nod for Libtayo in NSCLC: Regeneron Pharmaceuticals, Inc. (REGN - Free Report) and partner Sanofi (SNY - Free Report) obtained FDA approval for a label expansion of their PD-1 inhibitor, Libtayo (cemiplimab-rwlc). The drug is now approved for the first-line treatment of patients with advanced non-small-cell lung cancer (NSCLC) whose tumors have high PD-L1 expression (tumor proportion score ≥50%), as determined by an FDA-approved test. Libtayo was superior in extending overall survival compared to chemotherapy in a pivotal trial that allowed for certain disease characteristics frequently underrepresented in advanced NSCLC trials. Earlier this month, the drug was approved as the first immunotherapy for patients with advanced basal cell carcinoma (BCC) previously treated with a hedgehog pathway inhibitor (HHI) or for whom an HHI is not appropriate, with full approval granted for locally advanced disease and accelerated approval granted for metastatic disease.
Regeneron currently carries a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
Regulatory Updates From Incyte: Incyte (INCY - Free Report) announced that the FDA has accepted for Priority Review its supplemental New Drug Application (sNDA) for lead drug, Jakafi (ruxolitinib), for the treatment of steroid-refractory chronic graft-versus-host disease (GVHD) in adult and pediatric patients 12 years and older. The agency generally grants Priority Review to drugs that offer a major advancement in treatment where none currently exists. This designation shortens the review period to six months compared to 10 months for Standard Review. The target action date for this indication is Jun 22, 2021.
Separately, the agency has also accepted for Priority Review the New Drug Application (NDA) for ruxolitinib cream, a selective JAK1/JAK2 inhibitor designed for topical application, as a treatment for atopic dermatitis (AD), a type of eczema.
Nektar Up on Agreement With Merck: Shares of Nektar Therapeutics (NKTR - Free Report) gained after it announced an agreement with pharma giant Merck (MRK - Free Report) for a phase II/III study of the former’s bempegaldesleukin (NKTR-214, BEMPEG) in combination with the latter’s blockbuster immuno-oncology drug, Keytruda, for the first-line treatment of patients with metastatic or unresectable recurrent squamous cell carcinoma of the head and neck (SCCHN), whose tumors express PD-L1. Per the terms, Nektar will conduct the above-mentioned study, which is expected to enroll 500 patients with metastatic or recurrent SCCHN with PD-L1 expressing tumors. The company will conduct the above-mentioned study, which is expected to enroll 500 patients with metastatic or recurrent SCCHN with PD-L1 expressing tumors.
These patients will be randomized to receive either the combination of bempegaldesleukin and Keytruda or only Keytruda. The phase II portion of the study will include an interim analysis of the overall response rate (ORR) after the first 200 patients enrolled have a minimum follow-up of 4 months. The study will be continued only if the ORR passes a prespecified futility boundary.
Immunome Surges on Antibodies Update: Shares of Immunome, Inc. (IMNM - Free Report) surged after it announced that its discovery engine has isolated potent antibodies capable of neutralizing several SARS-CoV-2 variants, including the South African Variant (B.1.351), in pseudovirus testing. The company is developing a cocktail of antibodies targeting spike and non-spike proteins that can serve as a prophylaxis or treatment for COVID-19. Immunome has identified antibodies that bind to non-overlapping regions of the spike protein, including those regions containing the critical mutational variants while developing the antibody cocktail (IMM-BCP-001).
Otonomy Plunges on Study Data: Shares of Otonomy, Inc. plunged significantly after it announced that the late-stage study of Otividex was not successful. The phase III study of Otividex in patients with Ménière’s disease did not achieve the primary endpoint, which was the count of definitive vertigo days (DVD) in month 3 for Otividex as compared to placebo for the intent-to-treat (ITT) population (n = 148; p value = 0.312) using the Negative Binomial Model. The results did show statistical significance for the per protocol (PP) population.
Performance
Medical - Biomedical and Genetics Industry 5YR % Return
Medical - Biomedical and Genetics Industry 5YR % Return
The Nasdaq Biotechnology Index lost 4.20% in the last five trading sessions. Among the biotech giants, Vertex gained 2.93% during the period. Over the past six months, shares of Alexion have surged 49.3%. (See the last biotech stock roundup here: Biotech Stock Roundup: REGN’s Drug Approval & Pipeline Updates From AMGN, BLUE)
What's Next in Biotech?
Stay tuned for more pipeline and regulatory updates.
Biggest Tech Breakthrough in a Generation
Be among the early investors in the new type of device that experts say could impact society as much as the discovery of electricity. Current technology will soon be outdated and replaced by these new devices. In the process, it’s expected to create 22 million jobs and generate $12.3 trillion in activity.
A select few stocks could skyrocket the most as rollout accelerates for this new tech. Early investors could see gains similar to buying Microsoft in the 1990s. Zacks’ just-released special report reveals 8 stocks to watch. The report is only available for a limited time.
See 8 breakthrough stocks now>>