Candel Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Candel Therapeutics (Nasdaq: CADL) granted inducement stock options to three new employees under its 2025 Inducement Plan, adopted on December 24, 2025.
Rhea-AI Summary
Candel Therapeutics (Nasdaq: CADL) granted inducement stock options to three new employees under its 2025 Inducement Plan, adopted on December 24, 2025.
The awards cover an aggregate of 63,000 shares at an exercise price of $8.30 per share and were approved on May 31, 2026 under Nasdaq Listing Rule 5635(c)(4).
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Details
News Market Reaction – CADL
In the Jun 2 session, CADL declined 1.06%, reflecting a mild negative market reaction.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
- Inducement options granted
- 63,000 shares
- Aggregate stock options to three new employees under 2025 Inducement Plan
- Exercise price
- $8.30 per share
- Exercise price for inducement stock options granted May 31, 2026
- Initial vesting tranche
- 25% of shares
- Vests on first anniversary of each employee’s start date
- Remaining vesting schedule
- 75% over 36 months
- Vests in 36 equal monthly installments after first anniversary
- Plan adoption date
- December 24, 2025
- 2025 Inducement Plan adoption by Board
Historical Context
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Extended phase 3 CAN-2409 follow-up showed 39% disease-free survival improvement.
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Q1 2026 results, strong cash of $194.8M, and plans for BLA and NSCLC trial.
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CEO participation in Stifel oncology forum and Jefferies healthcare conference.
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Announcement of call to discuss extended phase 3 CAN-2409 prostate cancer data.
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Inducement options for 29,400 shares at $6.18 under 2025 Inducement Plan.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
stock options financial
Nasdaq Listing Rule 5635(c)(4) regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
NEEDHAM, Mass., June 01, 2026 (GLOBE NEWSWIRE) -- Candel Therapeutics, Inc. (Candel or the Company) (Nasdaq: CADL), a clinical-stage biopharmaceutical company focused on developing multimodal immunotherapies to improve disease outcomes for patients with cancer, today announced that on May 31, 2026, the Compensation Committee of Candel’s Board of Directors (the Board) granted to three new employees, stock options to purchase an aggregate of 63,000 shares of the Company’s common stock, with a per share exercise price of
The inducement stock options were made under the Company’s 2025 Inducement Plan (the Plan) and will vest with respect to
The above-described awards were each granted as inducement material to the employees entering into employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4) and were granted pursuant to the terms of the Plan. The Plan was adopted by the Board on December 24, 2025.
About Candel Therapeutics
Candel is a clinical-stage biopharmaceutical company focused on developing off-the-shelf multimodal biological immunotherapies that elicit an individualized, systemic anti-tumor immune response to help patients fight cancer. Candel has established two clinical-stage multimodal biological immunotherapy platforms based on novel, genetically modified adenovirus and herpes simplex virus (HSV) gene constructs, respectively. Aglatimagene besadenovec (CAN-2409 or aglatimagene) is the lead product candidate from the adenovirus platform. The Company recently completed successful phase 2a clinical trials of aglatimagene in non-small cell lung cancer (NSCLC) and pancreatic ductal adenocarcinoma (PDAC), and a pivotal, placebo-controlled, phase 3 clinical trial of aglatimagene in localized prostate cancer, conducted under a Special Protocol Assessment agreed with the U.S. Food and Drug Administration (FDA). The FDA also granted Fast Track Designation, Regenerative Medicine Advanced Therapy Designation to aglatimagene for the treatment of newly diagnosed localized prostate cancer in patients with intermediate-to-high-risk disease, Fast Track Designation in NSCLC, and both Fast Track Designation and Orphan Drug Designation to aglatimagene for the treatment of PDAC.
Linoserpaturev (CAN-3110) is the lead product candidate from the HSV platform and is currently in an ongoing phase 1b clinical trial in recurrent high-grade glioma, evaluating the effects of repeat linoserpaturev injections. Initial results were published in Nature and Science Translational Medicine and linoserpaturev received Fast Track Designation and Orphan Drug Designation from the FDA. Finally, Candel’s enLIGHTEN™ Discovery Platform is a systematic, iterative HSV-based discovery platform leveraging human biology and advanced analytics to create new viral immunotherapies for solid tumors.
For more information about Candel, visit: www.candeltx.com
Investor Contact
Theodore Jenkins
Vice President, Investor Relations and Business Development
Candel Therapeutics, Inc.
tjenkins@candeltx.com
Media Contact
Ben Shannon
ICR Healthcare
CandelPR@icrhealthcare.com
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