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Connect Biopharma Holdings CNTB · USD

Health Care · US listing · 🇺🇸 United States

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0.73

-0.41%

Close of 6 Nov 2026, in USD

About Connect Biopharma Holdings

From its filings with the US Securities and Exchange Commission

SEC filings

Connect Biopharma Holdings is based in San Diego, California and is incorporated in Cayman Islands. Its shares trade on Nasdaq under the ticker CNTB. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $64,000 and a net loss of $55.5m. At that date it held total assets of $56.1m and shareholders' equity of $42.0m.

In its own words

Connect Biopharma, headquartered in San Diego, California, is a clinical-stage biopharmaceutical company dedicated to transforming care for asthma and chronic obstructive pulmonary disease (“COPD”). The Company is advancing rademikibart, a next-generation, potentially best-in-class antibody designed to target interleukin-4-receptor alpha (“IL-4Rα”).

Asthma is a chronic inflammatory disease that affects the airways in the lungs and makes it difficult to breathe. It is one of the most common and costly diseases in the U.S., with an estimated 23 million adults and an estimated 5 million children suffering from asthma. Globally, asthma affected an estimated 262 million people in 2019 and caused 455,000 deaths. Asthma is associated with severe exacerbations that are difficult to treat and often require hospitalization. Approximately one million asthma patients visit emergency departments annually, of which approximately 11% are hospitalized with an average length-of-stay of two to three days. Approximately 50% of asthma patients who visit emergency departments meet treatment failure criteria within four weeks of an exacerbation. Approximately 20% of such patients require a re-visit to the emergency department and an additional approximately 30% require medical care from another source, such as urgent care or medical clinics. Current standard of care treatment for these patients includes fast-acting inhaled bronchodilators and oral or intravenous (“IV”) corticosteroids. Severe cases may require IV magnesium sulfate, heliox therapy, and noninvasive ventilation.

Quoted from its 10-K, filed 31 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
19 Mar 2021
Employees
64
Head office
3580 CARMEL MOUNTAIN ROAD, SUITE 200, SAN DIEGO, CA, 92130
Incorporated in
E9
Classification
Pharmaceutical Preparations
Filer status
<br>Emerging growth company

Leadership

Pay as last reported

  • Dr. Kleanthis XanthopoulosNon-Executive Independent Chairman of the Board$149,127
  • Mr. David SzekeresPresident$3.1m
  • Dr. Barry QuartChief Executive Officer and Director, since 2024$4.5m
  • Ms. Kimberly ManhardExecutive Vice President, Chief Development Officer
  • Ms. Lisa PerazaVice President - Finance$608,652
  • Mr. Raul CollazoVice President - Global Medical Affairs
  • Dr. Lei SunVice President - Biologics and Head of CMC
  • Mr. Jeff CohnGeneral Counsel and Corporate Secretary
  • Mr. James SchoeneckDirector
  • Mr. James HuangIndependent Director
  • Dr. Jean LiuIndependent Director$85,984
  • Ms. Karen WilsonIndependent Director$90,984

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

  • Headquartered in San Diego, California with a focus on biotechnology.
  • Operates as a clinical-stage biopharmaceutical company with a lead product candidate in development.
  • Completed a global Phase II trial for rademikibart in adult patients with moderate-to-severe AD.

Weaknesses

  • Employs only 62 full-time employees according to the source description.
  • IPO occurred in 2021, indicating a relatively new public company.
  • Relies on a single lead product candidate, rademikibart, for development.

Opportunities

  • Potential to advance rademikibart for asthma and COPD treatment after successful Phase II trials.
  • Focus on IL-4Rα antibody could address unmet needs in atopic dermatitis and asthma.
  • Clinical-stage status allows for further development and potential partnerships.

Threats

  • Dependence on a single product candidate may pose significant risk if development fails.
  • Biotechnology sector is highly competitive with many companies developing similar therapies.
  • Regulatory approval for rademikibart is required for market entry and commercialization.

Sources and methodology

Data on this tab
Our data supplier
Chart on the Overview
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