
EXPLORE HUMVIRA THERAPEUTICS
With Swiss quality, Powered by Basel spirit, Landed in Wuhan
Committed to
autologous HSCs mediated microgila replacement therapy
to address vastly unmet medical needs for a range of
rare hereditary disorders
MEDx GATEWAY
THINKING REVOLUTIONARILY FOR THE SOLUTION
​Find the condition you would like to address
Harness decades of research and advancements of the 4th generation of lentiviral mediated microgila replacement HSCs gene therapy to provide cures for a variety of genetic diseases through the approach of Medx Gateway
MUCOPOLYSACCHARIDOSIS
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Hurler Syndrome (MPSI)_alfa-L-iduronidase
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Hunter Syndrome (MPSII)_2-iduronate sulfatase
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Sanfilippo Syndrome (MPSIII A)_N-sulfoglucosamine sulfhydrolase
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Sanfilippo Syndrome (MPSIII B)_alfa-N-acetylglucosaminidase
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Sanfilippo Syndrome (MPSIII C)_acetyl-CoA:alfa-glucosamine acetyltransferase
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Sanfilippo Syndrome (MPSIII D)_N-acetylglucosamine 6-sulfatase
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Morquio Syndrome (MPSIV A)_N-acetylgalactosaminide 6-sulfatase
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Morquio Syndrome (MPSIV B)_beta-galactosidase-1
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Maroteaux Lamy Syndrome (MPSVI)_N-acetylgalactosamine 4-sulfatase
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Sly Syndrome (MPSVII)_beta-glucuronidase
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Hyaluronidase Deficiency (MPSIX)_hyaluronidase-1
SPHINGOLIPIDOSES
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Tay-Sachs Disease_beta-hexosaminidase A
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Sandhoff Disease_beta-hexosaminidase B
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Niemann-Pick Diseases A, B_acid sphingomyelinase
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Niemann-Pick Diseases C_NPC1 or NPC2
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Gaucher's Disease_beta-glucocerebrosidase
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Fabry's Disease_alfa-galactosidase A
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Metachromatic Leukodystrophy_arylsulfatase A
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Krabbe's Disease/Globoid Leukodystrophy_galactocerebrosidase
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GM1 Gangliosidosis_beta-galactosidase
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GM2 Gangliosidosis_GM2 ganglioside activator
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Austin Disease/Multiple Sulfatase Deficiency_multiple sulfatases
LIPOFUSCIN
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Batten Disease_PPT1
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Ceroid Lipofuscinosis 2_tripeptidyl peptidase
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Ceroid Lipofuscinosis 3_lysosomal transmembrane protein
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Parry Disease_CSPa
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Ceroid Lipofuscinosis 5_CLN-5
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Ceroid Lipofuscinosis 6_CLN-6
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Ceroid Lipofuscinosis 7_lysosomal membrane protein
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Ceroid Lipofuscinosis 8_CLN-8
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Ceroid Lipofuscinosis 9_unkown
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Ceroid Lipofuscinosis 10_cathepsin D
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Ceroid Lipofuscinosis 11_granulin precursor
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Ceroid Lipofuscinosis 12_cation-transporting ATPase 13A2
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Kufs Disease Yype B_cathepsin F
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Progressive Myoclonic Epilepsy_potassium channel tetramerization domain containing
MISCELLANEOUS
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Alfa Mannosidosis_alfa-mannosidase
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Beta-mannosidosis_beta-mannosidase
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Schindler Disease_alfa-N-acetylgalactosaminidase
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Aspartylglucosaminuria_aspartoglucosaminidase
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Fucosidosis_alfa-l-fucosidase
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Galactosialidosis_beta-galactosidase and neuraminidase
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Sialic Acid Storage Disease_sialin
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Mucolipidosis I_alfa-acetyl neuraminidase
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I-cell Disease_GlcNAc-1-phosphotransferase​
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Mucolipidosis IV_cation channel mucolipin 1
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Pompe Disease_acid maltase or acid alpha-glucosidase
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Danon Disease_LAMP-2
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Cystinosis_CTNS
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X-linked Adrenoleukodystrophy_ABCD1
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Action Myoclonus_LIMP-2
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Cobalamin F-type Disease_LMBD-1
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Angelman Syndrome_UBE3A
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Farber Lipogranulomatosis_acid ceramidase
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Wolman Disease_lysosomal acid lipase
Microgila replacement therapy
One-time treatment, Life-long impact
MEDx GATEWAY PIPELINES
Genetically corrected myeloid cells derived from engineered HSCs can migrate into the central nervous system, gradually replacing dysfunctional microglia and restoring function
—offering a durable and potentially curative solution.
