Aardvark Therapeutics Grants Stock Options to New Employees
Aardvark Therapeutics announced that on February 9, 2026, five new employees were granted inducement awards consisting of stock options to purchase an aggregate of 147,213 shares of common stock and on February 11, 2026, one new employee was granted an inducement award consisting of a stock option to purchase 5,125 shares of common stock. Each option was granted pursuant to the Aardvark Therapeutics, Inc. 2025 Inducement Equity Incentive Plan and was granted as an inducement material to each employee's employment with Aardvark in accordance with Nasdaq Listing Rule 5635(c)(4). The exercise price of each option is equal to the closing price of Aardvark's common stock on the date of grant, or $13.48 and $12.67 on February 9, 2026 and February 11, 2026, respectively. Each option will vest over four years, with 25% of the total number of shares vesting on the one-year anniversary of the date of commencement of such employee's employment with Aardvark and 1/48th of the total number of shares subject to each option vesting monthly thereafter, subject to continued employment.
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- Cardiac Observations: The therapeutic use of a certain treatment has been paused due to cardiac observations noted at above target doses.
- Safety Concerns: The decision to pause is likely driven by safety concerns related to the cardiac effects observed in patients.

Trial Overview: The article discusses the HERO and Open-Label Extension trials related to a therapeutic intervention.
Observations: It highlights that the trials are based on reversible cardiac observations above target doses.
- Investigation Launched: The Schall Law Firm is investigating Aardvark Therapeutics for potential violations of securities laws, focusing on whether the company issued false or misleading statements and failed to disclose critical information to investors.
- Trial Pause Reason: Aardvark announced the pause of its late-stage trial for a rare disease treatment due to heart-related side effects observed in healthy volunteers receiving higher-than-planned doses, indicating the company's cautious approach to safety monitoring.
- Stock Price Plunge: Following this news, Aardvark's shares fell by over 47.3% in after-hours trading, reflecting strong investor concerns about the company's future prospects and potentially leading to a decline in investor confidence.
- Investor Rights Protection: The Schall Law Firm encourages affected investors to reach out to discuss their rights, demonstrating the firm's proactive stance in protecting investor interests, which may lead to further legal actions.
- Trial Suspension Reason: Aardvark Therapeutics has voluntarily paused its Phase 3 HERO trial due to reversible cardiac observations identified during routine safety monitoring in a healthy volunteer study, indicating potential safety concerns at above-target therapeutic doses, prompting a comprehensive review of ARD-101's efficacy and safety.
- Data Release Delay: As a result of the trial suspension, Aardvark no longer expects to announce topline data from the HERO trial in Q3 2026, instead planning to provide updated guidance in Q2 of this year, reflecting the company's cautious approach to patient safety.
- Market Reaction: Aardvark's shares closed at $12.49, down $0.01 or 0.08% during regular trading, but sharply declined to $6.58 in after-hours trading, a drop of $5.91 or 47.32%, indicating market concerns regarding the company's future prospects.
- Enrollment and Dosing Halted: The company has suspended ongoing enrollment and dosing in the HERO trial while the evaluation is underway, demonstrating a strong commitment to clinical trial safety, which may impact its future R&D progress and market confidence.
- Trial Pause Reason: Aardvark Therapeutics announced a voluntary pause of its ARD-101 trial for Prader-Willi Syndrome due to cardiac observations in a healthy volunteer study, with data release now expected to be delayed until Q3 2026, potentially impacting the company's future R&D trajectory.
- Severe Market Reaction: Following the trial pause announcement, Aardvark's shares plunged 53% in after-hours trading, reflecting extreme investor concern over the company's outlook, which may lead to financing challenges and diminished market confidence.
- Competitor Dynamics: In contrast, Soleno Therapeutics' VYKAT XR has become the first FDA-approved treatment for hyperphagia in Prader-Willi Syndrome, despite facing short-selling pressure and safety concerns from Scorpion Capital, highlighting the intense competition in the market.
- Industry-Wide Challenges: Against the backdrop of Aardvark's trial pause, Acadia Pharmaceuticals also halted development of its intranasal Carbetocin, indicating that the challenges and risks associated with successful R&D in the Prader-Willi Syndrome treatment space are increasing, which could affect the overall investment attractiveness of the sector.
- Employee Incentive Program: Aardvark Therapeutics granted stock options totaling 152,338 shares to six new employees on February 9 and 11, 2026, aimed at attracting and retaining talent, thereby enhancing the company's competitive edge in the biopharmaceutical sector.
- Stock Option Details: The options were granted at exercise prices of $13.48 and $12.67, complying with Nasdaq Listing Rule 5635(c)(4), indicating the company's commitment to compliance and transparency in employee incentives.
- Long-Term Incentive Structure: Each option vests over four years, with 25% vesting in the first year and the remainder vesting monthly, designed to ensure employee commitment and stability, thus promoting sustained company growth.
- R&D Focus: Aardvark is dedicated to developing innovative therapies for metabolic diseases, particularly for Prader-Willi Syndrome, and the granting of stock options will help attract more specialized talent to advance its clinical trials and product development efforts.









