Last update 09 Dec 2025

Autologous Bone Marrow CD34+ Stem Cells (Emmes)

Overview

Basic Info

Drug Type
Hematopoietic stem cell therapy
Synonyms-
Target-
Action-
Mechanism
Stem cell replacements
Therapeutic Areas
Cardiovascular DiseasesEye Diseases
Active Indication-
Inactive Indication
Retinal Vein Occlusion
Originator Organization
The Emmes Co. LLCThe Emmes Co. LLC
Active Organization-
Inactive Organization
The Emmes Co. LLCThe Emmes Co. LLC
License Organization-
Drug Highest PhasePendingPhase 1/2
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with Autologous Bone Marrow CD34+ Stem Cells (Emmes)
NCT03981549
/ CompletedPhase 1/2
Phase I/II Randomized, Prospective, Double-masked, Sham-controlled Study of Intravitreal Autologous Bone Marrow CD34+ Stem Cell Therapy for Central Retinal Vein Occlusion
100 Clinical Results associated with Autologous Bone Marrow CD34+ Stem Cells (Emmes)
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100 Translational Medicine associated with Autologous Bone Marrow CD34+ Stem Cells (Emmes)
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100 Patents (Medical) associated with Autologous Bone Marrow CD34+ Stem Cells (Emmes)
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100 Deals associated with Autologous Bone Marrow CD34+ Stem Cells (Emmes)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Retinal Vein OcclusionPhase 2
United States
The Emmes Co. LLCThe Emmes Co. LLC
22 Oct 2019
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
NCT03981549 (TRUST, CTgov)
Phase 1/2
Retinal Vein Occlusion
16
(Immediate Cellular Therapy / Deferred Sham Therapy)
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-
02 Dec 2024
(Immediate Sham Therapy / Deferred Cellular Therapy)
aicaphvqzo = lzfzaxsouu iwyydnguco (eixnmqyzuk, oltmcrsbgg - kvsnccafws)
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Deal

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Approval

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Regulation

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