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Eledon Pharmaceuticals ELDN · USD

Health Care · US listing · 🇺🇸 United States

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2.87

+9.96%

Close of 9 Nov 2026, in USD

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About Eledon Pharmaceuticals

From its filings with the US Securities and Exchange Commission

SEC filings

Eledon Pharmaceuticals is based in Irvine, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker ELDN. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2016, it reported revenue of $0.

In its own words

Eledon is a clinical stage biotechnology company using our immunology expertise in targeting the CD40 Ligand (“CD40L”) pathway to develop therapies to protect transplanted organs and prevent rejection, and to treat amyotrophic lateral sclerosis (“ALS”). Our lead compound in development is tegoprubart, an IgG1, anti-CD40L antibody with high affinity for the CD40L, a well-validated biological target that we believe has broad therapeutic potential. We believe the central role of CD40L signaling in both adaptive and innate immune cell activation and function positions it as an attractive target for non-lymphocyte depleting, immunomodulatory therapeutic intervention.

Tegoprubart is engineered to potentially both improve safety and provide pharmacokinetic, pharmacodynamic, and dosing advantages compared to other anti-CD40 approaches. The CD40L/CD40 pathway is recognized for its prominent role in immune regulation. CD40L is primarily expressed on activated CD4+ T cells, platelets and endothelial cells while the CD40 receptor is constitutively expressed on antigen presenting cells such as macrophages and dendritic cells, as well as B cells. By blocking CD40L and not the CD40 receptor, tegoprubart inhibits both the CD40 and CD11 costimulatory signaling pathways, providing the potential for improved efficacy compared to anti-CD40 receptor approaches.

Quoted from its 10-K, filed 19 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
17 Sept 2014
Employees
33
Website
eledon.com ↗
Head office
19800 MACARTHUR BLVD., IRVINE, CA, 92612
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Mr. Keith KatkinIndependent Chairman of the Board$191,100
  • Dr. Steven PerrinPresident, Chief Scientific Officer, Director, since 2020$4.6m
  • Dr. David-Alexandre GrosChief Executive Officer, Director, since 2020$5.6m
  • Mr. Paul LittleChief Financial Officer$3.1m
  • Mr. Bryan SmithChief Compliance Officer, General Counsel, Corporate Secretary$1.7m
  • Dr. Jan HillsonIndependent Director$54,600
  • Dr. Allan KirkIndependent Director$61,080
  • Dr. June LeeIndependent Director$73,710
  • Mr. John McBrideIndependent Director, since 2014$72,345
  • Mr. James RobinsonIndependent Director$70,980

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
0
Environment
0
Social
0
Governance
0

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Eledon Pharmaceuticals focuses on the CD40L pathway for organ transplant treatments and autoimmune diseases.
  • Tegoprubart, an anti-CD40L antibody, offers improved safety and dosing advantages.
  • The company has a clinical stage development with a lead compound targeting ALS and autoimmune conditions.

Weaknesses

  • Eledon employs only 17 full-time employees in a clinical stage biotechnology sector.
  • The company's IPO in 2014 has not yet resulted in commercialized products.
  • Eledon's lead compound is still in development without approved treatments.

Opportunities

  • The growing market for autoimmune disease treatments presents a significant opportunity for Eledon.
  • The CD40L pathway research could expand into new therapeutic areas beyond current focus.
  • Eledon's technology may attract partnerships with larger pharmaceutical companies.

Threats

  • Competition from established biotech firms in the CD40L pathway research space is increasing.
  • Regulatory hurdles for new biologics could delay product approvals.
  • The high costs of clinical trials may strain the company's limited resources.

Sources and methodology

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