Armagen Inc.
914 Colorado Avenue
Santa Monica
California
90401
United States
Tel: 310-917-1275
Fax: 310-917-1276
Website: http://www.armagen.com/
Email: contact@armagen.com
24 articles about Armagen Inc.
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JCR Pharmaceuticals announces Completion of Acquisition of ArmaGen, Inc.
4/27/2020
JCR Pharmaceuticals Co., Ltd. announced that it has completed the previously announced acquisition of ArmaGen, Inc., a privately held US biopharmaceutical company headquartered in San Diego, California.
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ArmaGen Receives U.S. Orphan Drug Designation for AGT-184
8/2/2018
Novel Enzyme Replacement Therapy in Development for the Treatment of Sanfilippo A Syndrome
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ArmaGen's AGT-181 52-Week Phase 1/2 Proof-of-Concept Study Results Published in Orphanet Journal of Rare Diseases
7/10/2018
Novel Fusion Protein Demonstrates Neurocognitive Benefit in Children with Severe Mucopolysaccharidosis Type I (MPS I, or Hurler Syndrome), with Favorable Safety Profile
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ArmaGen's AGT-181 Demonstrates Neurocognitive Benefit in Children With Severe MPS I
2/9/2018
On a somatic level, AGT-181 stabilized urinary glycosaminoglycans, reduced liver and spleen volume including in patients previously exposed to laronidase, and further improved shoulder range of motion.
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ArmaGen's AGT-181 Granted Fast Track Designation for the Treatment of Hurler Syndrome (MPS I)
11/30/2017
The data suggested that AGT-181 improves neurocognitive function in patients with MPS I, demonstrating the ability of ArmaGen's proprietary drug delivery technology to transport biopharmaceuticals across the blood-brain barrier.
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ArmaGen Reports Preliminary Evidence Of Cognitive Improvement In Children With Hurler Syndrome (MPS I) Treated With AGT-181
2/17/2017
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ArmaGen CEO: Phase II Data Shows Cognitive Improvement in Juvenile Hurler Syndrome Patients
2/16/2017
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ArmaGen Technologies, Inc. Release: Company Appoints Mathias Schmidt, Ph.D., As Chief Executive Officer
1/19/2017
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ArmaGen Technologies, Inc. And Rett Syndrome Research Trust Collaborate To Develop Novel Therapeutic For The Treatment Of Rett Syndrome
7/7/2016
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ArmaGen Technologies, Inc. Announces Initiation Of Phase 2 Proof-Of-Concept Clinical Trial In Brazil To Study AGT-181 For The Treatment Of Hurler Syndrome
3/31/2016
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ArmaGen Technologies, Inc. Receives Rare Pediatric Disease Designation From FDA For AGT-181 For The Potential Treatment Of Hurler Syndrome (Mucopolysaccharidosis Type I)
11/5/2015
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ArmaGen Technologies, Inc. Announces First Patient Dosed In Phase 1/2a Clinical Trial Of AGT-181 For The Treatment Of Hurler Syndrome
9/2/2015
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ArmaGen Technologies, Inc. Achieves Clinical Milestone In Hunter Syndrome Collaboration With Shire
6/15/2015
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ArmaGen Technologies, Inc. Announces FDA Acceptance Of IND Application For AGT-181 For The Treatment Of Hurler Syndrome
4/8/2015
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PacificGMP And ArmaGen Technologies, Inc. Announce Successful Manufacture Of Armagen's Investigational Enzyme Replacement Therapies, AGT-182 And AGT-181, For Phase 1 Clinical Trial
3/10/2015
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ArmaGen Technologies, Inc. To Present At Oppenheimer 25th Annual Healthcare Conference
12/5/2014
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ArmaGen Technologies, Inc. Licenses AGT-182 Rights To Shire For Up To $225M
7/23/2014
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ArmaGen Technologies, Inc. Receives Notice Of Allowance For U.S. Patent Covering Novel Investigational Therapy For Hunter Syndrome
6/17/2014
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ArmaGen Technologies, Inc. Expands Patent Portfolio With Issuance of Two Additional U.S. Patents
9/4/2013
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ArmaGen Technologies, Inc. Receives US Orphan Designation for Lead Product AGT-182
7/19/2013