biomarin pharmaceutical inc products

Call your doctor for medical advice about side effects. Details BioMarin is a global pharmaceutical company focused on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients … Jean-Jacques Bienaimé - Chairman and … Inform patients/caregivers of the signs and symptoms of anaphylaxis and to seek immediate medical care should these occur. PALYNZIQ ® (pegvaliase-pqpz) Injection; Brineura ® (cerliponase alfa) Vimizim ® (elosulfase alfa) Kuvan ® (sapropterin dihydrochloride) Naglazyme ® (galsulfase) Aldurazyme ® … BioMarin Pharmaceutical Inc. Biotechnology San Rafael, CA 83,874 followers We bring new treatments to market that will make a big impact on small patient populations. Get directions, reviews and information for BioMarin Pharmaceutical Inc in Indian Rocks Beach, FL. Safety and effectiveness in pediatric patients below 3 years of age have not been established. Consider the risks and benefits of readministration of Brineura following an anaphylactic reaction. PALYNZIQ ® (pegvaliase-pqpz) Injection for PKU; Brineura ® (cerliponase alfa) for CLN2 Disease; Vimizim ® (elosulfase alfa) for Morquio A Syndrome (MPS IVA); Kuvan ® (sapropterin … The Company has applied its proprietary enzyme technology to develop products … For more information, please see our, Valoctocogene Roxaparvovec for Severe Hemophilia A, PALYNZIQ® (pegvaliase-pqpz) Injection for PKU, Kuvan® (sapropterin dihydrochloride) for PKU, Brineura® (cerliponase alfa) for CLN2 Disease, Vimizim® (elosulfase alfa) for Morquio A Syndrome (MPS IVA), BioMarin Announces Positive Phase 3 Gene Therapy Trial Results in Adults with Severe Hemophilia A; Study Met All Primary and Secondary Efficacy Endpoints in One-Year Data Set, BioMarin to Participate in Two Upcoming Virtual Investor Conferences, BioMarin Announces Benefit Maintained for Over Two Years in Children with Achondroplasia Treated with Vosoritide in Phase 3 Extension Study, BioMarin and Deep Genomics to Collaborate on Advancing Programs Identified Using Artificial Intelligence, BioMarin to Participate in Three Upcoming Virtual Investor Conferences, BioMarin Expands Vosoritide Clinical Program, BioMarin Announces Third Quarter 2020 Total Revenues of $477 Million. Each drug candidate we pursue is guided by a fundamental understanding of the genetics and underlying biology of the condition it will address. Reviews (415) 506-6700 Website. CLN2 disease is an ultra-rare and rapidly progressing brain disorder that affects an estimated 20 children born in the United States each year–less than one in a million Americans. Our thoughtful approach to clinical trial design enables us to move fast and efficiently while protecting the safety of our patients. BioMarin … Before treatment with Brineura, it is important to discuss your child’s medical history with their doctor. For more information, please see our, Valoctocogene Roxaparvovec for Severe Hemophilia A, PALYNZIQ® (pegvaliase-pqpz) Injection for PKU, Kuvan® (sapropterin dihydrochloride) for PKU, Vimizim® (elosulfase alfa) for Morquio A Syndrome (MPS IVA). The Company has applied its proprietary enzyme technology to develop products for lysosomal storage … Brineura is the first enzyme replacement therapy to be directly administered into the fluid of the brain, treating the underlying cause of CLN2 disease by helping to replace the deficient TPP1 enzyme missing in affected children. ... Pharmaceutical Products Wholesale Pharmaceutical Products … PALYNZIQ ® (pegvaliase-pqpz) Injection for PKU; Brineura ® (cerliponase alfa) for CLN2 Disease; Vimizim ® (elosulfase alfa) for Morquio A Syndrome (MPS IVA) Kuvan ® (sapropterin … Contents: Prepared Remarks; Questions and Answers; Call Participants; Prepared … This website uses cookies to improve website functionality. SAN RAFAEL, Calif., Jan. 10, 2021 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) today announced positive topline results from its ongoing global Phase 3 GENEr8 … This BioMarin process requires an in person interview at one of our company locations and never requires payment or fees from job applicants. Phase (Preclinical, Phase 1, Phase 2, Phase 3, BLA/NDA/MAA, Approval), Brineura® (cerliponase alfa) for CLN2 Disease, This website uses cookies to improve website functionality. Intraventricular device-related side effects included infection, delivery system-related complications, and increased white blood cell count in fluid of the brain. If a reaction occurs, the infusion will be stopped and your child may be given additional medication. As of December 31, 2016, the … BioMarin Pharmaceuticals develops drugs with a focus on rare disease treatments. Low blood pressure and/or slow heart rate may occur during and following the Brineura infusion. Traci McCarty - VP, IR. Tell the doctor if they are sick or taking any medication and if they are allergic to any medicines. If any signs of anaphylaxis occur, immediately seek medical care. BioMarin Pharmaceutical Inc. (BMRN Quick Quote BMRN - Free Report) BioMarin announced one-year follow-up data from a phase III study on its pipeline candidate, valoctocogene … If you have questions or would like more information about Brineura, contact your child’s doctor. BioMarin sells multiple drugs for rare diseases, but valrox is its first legitimate chance to have a blockbuster treatment with more than $1 billion in sales. Biomarin Pharmaceutical Inc ... With six highly innovative products developed, approved and commercialized for a variety of rare conditions over the last two decades, this is familiar … The company's Vimizim, Naglazyme, and Aldurazyme drugs treat versions of the life-threatening genetic condition … BioMarin Pharmaceutical Inc. develops and commercializes therapeutic enzyme products. Intraventricular access device-related infections, including meningitis, were observed with Brineura treatment. Our Products. BioMarin Pharmaceutical Inc. (NASDAQ:BMRN) Q3 2020 Earnings Conference Call November 5, 2020 4:30 PM ET Company Participants. BioMarin Pharmaceutical, Inc. is a biotechnology company, which engages in the development and commercialization of therapies for people with serious and life-threatening rare … Undesirable or hypersensitivity reactions related to Brineura treatment, including fever, vomiting, and irritability, may occur during treatment and as late as 24 hours after infusion. If a severe reaction occurs, the infusion will be stopped and your child will receive appropriate medical treatment. Your doctor should vigilantly be looking for signs and symptoms of infection, including meningitis, during treatment with Brineura. PALYNZIQ® (pegvaliase-pqpz) Injection for PKU; Kuvan® (sapropterin dihydrochloride) for PKU; Brineura® (cerliponase alfa) for CLN2 Disease; ALDURAZYME® (laronidase) for MPS I; … You may delete or block cookies by accessing your preferences. BioMarin Pharmaceutical Inc 307 12th Ave Indian Rocks Beach FL 33785. Serious and severe allergic reactions (anaphylaxis) may occur. You may delete or block cookies by accessing your preferences. Please note that any opinions, estimates or forecasts regarding BioMarin Pharmaceutical Inc.'s performance made by these analysts are theirs alone and do not represent opinions, forecasts or predictions of BioMarin Pharmaceutical Inc. or its management. The Company develops and commercializes pharmaceuticals for various diseases and medical conditions. BioMarin Pharmaceutical Inc. has collaboration and license agreements with Sarepta Therapeutics and Asubio Pharma Company; and a preclinical collaboration and license agreement with DiNAQOR AG … These are not all of the possible side effects with Brineura. Biomarin Pharmaceutical Inc ... commercial products and potential future products in different areas of therapeutic research and development. Contact your child’s doctor immediately if these reactions occur. Brineura is a prescription medicine. BioMarin Pharmaceutical Inc BioMarin Pharmaceutical Inc. develops and commercializes therapeutic enzyme products. BioMarin Pharmaceutical Inc. is a biotechnology company. cellulitis or abscess), or and with shunts used to drain extra fluid around the brain. Our Products. Each drug candidate we pursue is guided by a fundamental understanding of the genetics and underlying biology of the condition it will address. Your child’s doctor should inspect the scalp and collect samples of your child’s cerebrospinal fluid (CSF) prior to each infusion of Brineura, to check that there is no device failure or infections present. BioMarin Pharmaceutical Inc. is a biotechnology company. Brineura is only given by infusion into the fluid of the brain (known as an intraventricular injection) and using sterile technique to reduce the risk of infection. Your child’s doctor will decide if Brineura is right for them. BioMarin Pharmaceutical Inc. Brineura should not be used in patients with active intraventricular access device-related complications (e.g., leakage, device failure, or device-related infection, including meningitis), symptom of acute, unresolved localized infection around the device insertion site (e.g. BioMarin Pharmaceutical Inc. 770 Lindaro Street San Rafael, CA 94901 At BioMarin, we focus on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. BioMarin Pharmaceutical Inc… An intraventricular access device or port must be in place at least 5 to 7 days prior to the first infusion. Your child may receive medication such as antihistamines before Brineura infusions to reduce the risk of reactions. Our Products. The Company develops and commercializes pharmaceuticals for various diseases and medical conditions. SAN RAFAEL, Calif., Dec. 21, 2020 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) today announced that children in the open-label long-term extension of the Phase … BioMarin Pharmaceutical Inc. 770 Lindaro Street San Rafael, CA 94901 Directions › Tel: +1 (415) 506-6700 E-mail: Media Relations E-mail: Investor Relations *Please direct all mail to the U.S. mailing … ... Its commercial products … We are committed to developing safe and effective therapies and providing those therapies to the broadest group of patients as quickly as possible. The signs and symptoms of infections may not be readily apparent in patients with CLN2 disease. In the event you receive a suspicious email message about recruiting on behalf of BioMarin… We are committed to the communities we treat beyond the therapies we develop. Our Products. Your child’s intraventricular access device should be replaced prior to 4 years of single-puncture administration of Brineura, because the device may deteriorate due to repeated use. Please see accompanying full Prescribing Information, or visit www.Brineura.com. As of 2016, BioMarin has six products on the market, each of which is an orphan drug. Biomarin Pharmaceutical Inc (NASDAQ:BMRN) Q2 2020 Earnings Call Aug 4, 2020, 4:30 p.m. You may report side effects to BioMarin Pharmaceutical Inc. at 1-866-906-6100, or the FDA at 1-800-FDA-1088 or go to www.fda.gov/medwatch. If anaphylaxis occurs, immediately discontinue infusion and initiate appropriate medical treatment. ET. The most common side effects reported during Brineura infusions included fever, problems with the electrical activity of the heart, decreased or increased protein in the fluid of the brain, vomiting, seizures, hypersensitivity, collection of blood outside of blood vessels (hematoma), headache, irritability, and increased white blood cell count in the fluid of the brain, device-related infection, slow heart rate, feeling jittery, and low blood pressure. BioMarin Pharmaceutical Inc’s price can fluctuate throughout the course of each trading day—when you buy BioMarin Pharmaceutical Inc through Stash, we execute the market order during our next … Results may differ materially depending on … Talk to your child’s doctor if they have any symptoms that bother them or that do not go away. Brineura® (cerliponase alfa) is indicated to slow the loss of ambulation in symptomatic pediatric patients 3 years of age and older with late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), also known as tripeptidyl peptidase 1 (TPP1) deficiency. Due to the potential for anaphylaxis, appropriate medical support should be readily available, and patients should be observed closely, during and after Brineura infusion. Brineura® (cerliponase alfa) is a prescription medication used to slow loss of ability to walk or crawl (ambulation) in symptomatic pediatric patients 3 years of age and older with late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), also known as tripeptidyl peptidase 1 (TPP1) deficiency. If any signs of infection or meningitis occur, contact your child’s doctor immediately. Your child may be given additional medication biology of the condition it will address infusion and initiate medical! Infection, including meningitis, were observed with Brineura us to move fast and efficiently while protecting the safety our. And medical conditions appropriate medical treatment candidate we pursue is guided by a understanding. With shunts used to drain extra fluid around the brain medical advice about side effects included,! Vigilantly be looking for signs and symptoms of infections may not be readily apparent patients... 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