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GENERATION BIO*

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Mark	Details	Status	Class/Description
	GENERATION BIO GENERATION BIO CO. 1897866 7 May 2018	REGISTERED on 18 May 2021	Pharmaceutical preparations and genetic medicines for the treatment of... Class 005 Class 005 Pharmaceutical Products Pharmaceutical preparations and genetic medicines for the treatment of genetic disorders, genetic diseases, related diseases having a genetic cause or component and disease states resulting from gene expression or genetic sequence, namely, Hemophilia A, hemophilia B, cystic fibrosis, familial hypercholesterolemia, phenylketonuria, Wilson's disease, congenital hepatic porphyria, Lesch-Nyhan syndrome, Leber Congenital Amaurosis, Stargardt macular dystrophy, ornithine transcarbamylase deficiency, Usher syndrome, alpha-1 antitrypsin deficiency, progressive familial intrahepatic cholestasis types I, II, III, and IV, sickle cell anemia, thalassaemias, xeroderma pigmentosum, Fanconi's anemia, retinitis pigmentosa, macular degeneration, ataxia telangiectasia, Bloom's syndrome, retinoblastoma, Hurler syndrome, Scheie syndrome, Hurler-Scheie syndrome, Hunter syndrome, Sanfilippo Types A, B, C, and D, Morquio Types A and B, Maroteaux-Lamy syndrome, Sly syndrome, hyaluronidase deficiency, Niemann-Pick Disease Types A, B, C1 and C2, Fabry disease, Schindler disease, Sandhoff Disease, Tay-Sachs disease, Metachromatic Leukodystrophy, Krabbe disease, Mucolipidosis Type I, II, III and IV, Sialidosis Types I and II, glycogen storage disease Types I and II, Gaucher disease Types I, II and III, cystinosis, Batten disease, Aspartylglucosaminuria, Salla disease, Danon disease, Lysosomal Acid Lipase deficiency, Pompe disease, neuronal ceroid lipofuscinoses, sphingolipidosis, galactosialidosis, amyotrophic lateral sclerosis, Parkinson's disease, Alzheimer's disease, Huntington's disease, spinocerebellar ataxia, spinal muscular atrophy, Friedreich's ataxia, Duchenne muscular dystrophy, Becker muscular dystrophies, dystrophic epidermolysis bullosa, ectonucleotide pyrophosphatase 1 deficiency, generalized arterial calcification of infancy, and cathepsin A deficiency. Class 042 Class 042 Computer & Software Services & Scientific Services Scientific and medical research relating to the diagnosis and/or treatment of genetic diseases and related diseases; product development and consultancy in the field of biotechnology, biologics, pharmaceutics, medical science, chemistry and biochemistry. ... Class 044 Medical, Beauty & Agricultural Services Providing information in the field of diagnosis and/or treatment of genetic diseases and related diseases; therapeutic gene and nucleic acid delivery, gene and nucleic acid transfer, gene and nucleic acid regulation and gene and nucleic acid modulation for the treatment of genetic diseases and related diseases, via website
	GENERATION BIO & DESIGN GENERATION BIO CO. 1897867 7 May 2018	REGISTERED on 18 May 2021	Pharmaceutical preparations and genetic medicines for the treatment of... Class 005 Class 005 Pharmaceutical Products Pharmaceutical preparations and genetic medicines for the treatment of genetic disorders, genetic diseases, related diseases having a genetic cause or component and disease states resulting from gene expression or genetic sequence, namely, Hemophilia A, hemophilia B, cystic fibrosis, familial hypercholesterolemia, phenylketonuria, Wilson's disease, congenital hepatic porphyria, Lesch-Nyhan syndrome, Leber Congenital Amaurosis, Stargardt macular dystrophy, ornithine transcarbamylase deficiency, Usher syndrome, alpha-1 antitrypsin deficiency, progressive familial intrahepatic cholestasis types I, II, III, and IV, sickle cell anemia, thalassaemias, xeroderma pigmentosum, Fanconi's anemia, retinitis pigmentosa, macular degeneration, ataxia telangiectasia, Bloom's syndrome, retinoblastoma, Hurler syndrome, Scheie syndrome, Hurler-Scheie syndrome, Hunter syndrome, Sanfilippo Types A, B, C, and D, Morquio Types A and B, Maroteaux-Lamy syndrome, Sly syndrome, hyaluronidase deficiency, Niemann-Pick Disease Types A, B, C1 and C2, Fabry disease, Schindler disease, Sandhoff Disease, Tay-Sachs disease, Metachromatic Leukodystrophy, Krabbe disease, Mucolipidosis Type I, II, III and IV, Sialidosis Types I and II, glycogen storage disease Types I and II, Gaucher disease Types I, II and III, cystinosis, Batten disease, Aspartylglucosaminuria, Salla disease, Danon disease, Lysosomal Acid Lipase deficiency, Pompe disease, neuronal ceroid lipofuscinoses, sphingolipidosis, galactosialidosis, amyotrophic lateral sclerosis, Parkinson's disease, Alzheimer's disease, Huntington's disease, spinocerebellar ataxia, spinal muscular atrophy, Friedreich's ataxia, Duchenne muscular dystrophy, Becker muscular dystrophies, dystrophic epidermolysis bullosa, ectonucleotide pyrophosphatase 1 deficiency, generalized arterial calcification of infancy, and cathepsin A deficiency. Class 042 Class 042 Computer & Software Services & Scientific Services Scientific and medical research relating to the diagnosis and/or treatment of genetic diseases and related diseases; product development and consultancy in the field of biotechnology, biologics, pharmaceutics, medical science, chemistry and biochemistry ... Class 044 Medical, Beauty & Agricultural Services Providing information in the field of diagnosis and/or treatment of genetic diseases and related diseases; therapeutic gene and nucleic acid delivery, gene and nucleic acid transfer, gene and nucleic acid regulation and gene and nucleic acid modulation for the treatment of genetic diseases and related diseases, via website

REGISTERED

on 18 May 2021

GENERATION BIO

GENERATION BIO CO.

1897866 · 7 May 2018

005

042

...

Pharmaceutical preparations and genetic medicines for the treatment of...

REGISTERED

on 18 May 2021

GENERATION BIO & DESIGN

GENERATION BIO CO.

1897867 · 7 May 2018

005

042

...

Pharmaceutical preparations and genetic medicines for the treatment of...

Owners

Generation bio co. (2)

Categories

Class 5 (2)

Class 42 (2)

Class 44 (2)

Correspondents

Smart & biggar lp (2)

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