BMRN Share Price

Open 87.65 Change Price %
High 88.65 1 Day 0.67 0.77
Low 87.65 1 Week -1.23 -1.38
Close 88.00 1 Month -8.26 -8.58
Volume 933838 1 Year -1.09 -1.22
52 Week High 102.49
52 Week Low 73.45
BMRN Important Levels
Resistance 2 88.93
Resistance 1 88.55
Pivot 88.10
Support 1 87.46
Support 2 87.07
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BioMarin Pharmaceutical Inc. (NASDAQ: BMRN)

BMRN Technical Analysis 4
As on 26th May 2017 BMRN Share Price closed @ 88.00 and we RECOMMEND Sell for LONG-TERM with Stoploss of 89.66 & Strong Sell for SHORT-TERM with Stoploss of 90.49 we also expect STOCK to react on Following IMPORTANT LEVELS.
BMRN Target for May
1st Target up-side 103.2
2nd Target up-side 108.35
3rd Target up-side 113.51
1st Target down-side 88.48
2nd Target down-side 83.33
3rd Target down-side 78.17
BMRN Other Details
Segment EQ
Market Capital 6022899712.00
Sector Healthcare
Industry Biotechnology
Offical website
BMRN Address
770 Lindaro Street
San Rafael, CA 94901
United States
Phone: 415-506-6700
Fax: 415-382-7889
BMRN Latest News
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BMRN Business Profile
BioMarin Pharmaceutical Inc. (BioMarin), incorporated in October 25, 1996, develops and commercializes pharmaceuticals for serious diseases and medical conditions. The Company’s product portfolio is comprised of four approved products and multiple investigational product candidates. Approved products include Naglazyme (galsulfase), Kuvan (sapropterin dihydrochloride), Aldurazyme (laronidase) and Firdapse (amifampridine phosphate). It is conducting clinical trials on several product candidates for the treatment of various diseases. They include Vimizim (formerly referred to as GALNS), an enzyme replacement therapy for the treatment of Mucopolysaccharidosis Type IV or Morquio Syndrome Type A (MPS IV A), PEG-PAL, an enzyme substitution therapy for the treatment of phenylketonuria (PKU), BMN-701, an enzyme replacement therapy for Pompe disease, a glycogen storage disorder, BMN-673, an orally available poly (ADP-ribose) polymerase, or PARP inhibitor for the treatment of patients with certain cancers and BMN-111, a peptide therapeutic for the treatment of achondroplasia. On January 7, 2013, the Company acquired Zacharon Pharmaceuticals. The Company is conducting or planning to conduct preclinical development of several other enzyme product candidates for genetic and other metabolic diseases, including BMN-190 for the treatment of late infantile neuronal ceroid lipofuscinosis (LINCL), a form of Batten disease. The Company is developing Vimizim, an enzyme replacement therapy for the treatment of MPS IV A, a lysosomal storage disorder. PEG-PAL is an investigational enzyme substitution therapy that it is developing as a subcutaneous injection for the treatment of PKU. In preclinical models, PEG-PAL produced a rapid, dose-dependent reduction in blood phenylalanine (Phe) levels. BMN-673 is a PARP inhibitor, which is a class of molecules that has shown clinical activity against cancers involving defects in deoxyribonucleic acid (DNA) repair that it is investigating for the treatment of certain cancers. BMN-701 is a fusion of insulin-like growth factor 2 and alpha glucosidase (IGF2-GAA) in development for Pompe disease. Pompe disease is a lysosomal storage disorder caused by a deficiency in GAA, which prevents cells from adequately degrading glycogen. BMN-111 is a peptide therapeutic in development for the treatment of achondroplasia. The Company manufactures Naglazyme, Aldurazyme, Vimizim, PEG-PAL and BMN-111 in its production facilities located in Novato, California. Vialing and packaging are performed by contract manufacturers. Kuvan is manufactured on a contract basis by a third-party. Its Naglazyme, Kuvan and Firdapse customers include a limited number of specialty pharmacies and end-users, such as hospitals and foreign government agencies, which act as retailers. The Company also sells Naglazyme to its authorized European distributors and to certain pharmaceutical wholesalers.