Clinical development failure
EB613, EB612 and oral OXM are still in development and may not demonstrate safety or efficacy.
- Scope
- Lead pipeline programs
- Materiality
- high
Entera Bio Ltd. is a clinical-stage biotechnology company developing oral tablet versions of peptide and protein replacement therapies. Its lead work centers on the N-Tab platform and first-in-class oral programs in osteoporosis and metabolic disease, including EB613, EB612, and oral GLP-1/GLP-2-related candidates.
−27 378,6 %
−27 235,7 %
−76,8 %
6.94
6.94
| % | |
|---|---|
| Oral peptide therapeutics | 0% Development of oral tablet formulations designed to replace injectable peptide and protein therapies. |
| Lead clinical programs | 0% EB613, EB612 and oral OXM programs targeting osteoporosis and metabolic disease. |
| Platform technology | 0% N-Tab™ delivery technology used to enable oral administration of biologics. |
| Collaborative research services | 100% Contract research and material transfer services performed for third parties. |
Entera does not yet sell approved products to commercial end customers; its current economic counterparties are...
Third parties that pay for material transfer and research services while Entera performs contract R&D work.
Potential users of EB613 if approved, seeking an oral alternative to injectable PTH therapy.
Potential users of oral GLP-1/Glucagon or GLP-2 therapies if the programs reach commercialization.
Partners that may license, co-develop, or fund oral peptide programs to access the platform.
Entera’s operations are centered in Jerusalem, Israel, where all employees are based and core R&D work is performed...
Entera is focused on advancing first-in-class oral versions of peptide therapies that are normally delivered by...
EB613 is the most advanced program and could validate the platform in a large osteoporosis market.
The collaboration can expand the pipeline into metabolic disease while sharing development burden.
Platform validation across multiple peptides can improve partnering leverage and long-term optionality.
Clinical development requires capital and the company has stated additional funding will be needed.
Entera is a pre-revenue clinical-stage company, so execution risk is concentrated in clinical outcomes, regulatory...
EB613, EB612 and oral OXM are still in development and may not demonstrate safety or efficacy.
The company expects to need additional capital before commercialization and may not raise it on favorable terms.
Employees and operations are based in Israel, so conflict could disrupt work, supply chains, or fundraising.
The company needs FDA and other regulatory alignment before advancing into later-stage trials and approval.
Development timelines and economics depend partly on third-party collaboration agreements.
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