Fennec Pharmaceuticals Showcases PEDMARK Research at ASCO Meeting
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Apr 21 2026
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Source: Newsfilter
- Clinical Research Highlights: Fennec Pharmaceuticals announced that four abstracts on PEDMARK® were accepted for the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, showcasing the drug's potential in preventing cisplatin-induced ototoxicity, which is expected to enhance the company's market position in oncology.
- Drug Indication: PEDMARK® is FDA-approved for pediatric patients aged one month and older to reduce the risk of ototoxicity associated with cisplatin treatment, receiving a 2A recommendation from the National Comprehensive Cancer Network (NCCN), underscoring its significance in pediatric oncology.
- Presentation Schedule: The four studies will be presented at the ASCO meeting from May 29 to June 2, 2026, including randomized trials for various cancer patients, which are anticipated to attract industry attention and drive the market promotion of PEDMARK.
- Impact of Ototoxicity: Ototoxicity affects 60-90% of patients treated with cisplatin, and the introduction of PEDMARK offers a new treatment option for these patients, expected to improve quality of life and reduce long-term healthcare costs.
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Analyst Views on FENC
Wall Street analysts forecast FENC stock price to rise
4 Analyst Rating
4 Buy
0 Hold
0 Sell
Strong Buy
Current: 8.980
Low
13.00
Averages
14.67
High
18.00
Current: 8.980
Low
13.00
Averages
14.67
High
18.00
About FENC
Fennec Pharmaceuticals Inc. is a commercial-stage biopharmaceutical company focused on its product candidate, PEDMARK. It sells its product through a field force, including Regional Pediatric Oncology Specialists and medical science liaisons who are helping to educate the medical communities and patients about cisplatin induced ototoxicity and its programs supporting patient access to PEDMARK. PEDMARK is an approved therapy indicated to reduce the risk of ototoxicity associated with cisplatin treatment in pediatric patients with localized, non-metastatic, solid tumors. It is a formulation of sodium thiosulfate in single-dose, ready-to-use vials for intravenous use in pediatric patients. PEDMARK is a therapeutic agent with a dosing paradigm, across two open-label, randomized Phase III clinical studies, the Clinical Oncology Group (COG) Protocol ACCL0431 and SIOPEL 6. It has established Fennec HEARS, a single source program designed to connect PEDMARK patients.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Stock Option Grant: On June 10, 2026, Fennec Pharmaceuticals approved the grant of 10,000 incentive stock options to a new non-executive employee, with an exercise price of $9.00 per share, reflecting the company's commitment to attracting talent to strengthen its team for future business growth.
- Inducement Plan Context: The stock options were granted under Nasdaq Listing Rule 5635(c)(4) to attract individuals who were not previously employed by the company, indicating a strategic focus on talent acquisition to enhance competitiveness in the pharmaceutical industry.
- Stock Option Structure: The granted stock options will vest in three installments over the first year, followed by monthly vesting, ensuring employee retention and loyalty, which is crucial for maintaining a stable workforce.
- Product Commercialization Progress: Fennec is focused on the commercialization of PEDMARK®, which has received FDA and European Commission approvals, and the addition of new employees is expected to accelerate market penetration, thereby increasing the company's market share in the oncology drug sector.
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- Director Election Results: At the Annual General Meeting on June 10, 2026, Fennec Pharmaceuticals elected five directors, with Khalid Islam receiving 97.84% support, indicating strong shareholder confidence in management.
- Auditor Appointment: Shareholders voted 99.64% in favor of appointing Haskell & White LLP as auditors, reflecting a commitment to audit quality while authorizing the board to determine auditor remuneration, ensuring financial transparency.
- Executive Compensation Approval: 85.50% of shareholders approved the compensation for the company's executives, demonstrating recognition of corporate governance and the incentive structure aimed at attracting and retaining key talent.
- Equity Incentive Plan Amendment: 91.27% of shareholders supported amendments to the 2020 Equity Incentive Plan, indicating backing for long-term incentive measures, with a support rate of 88.01% after excluding shares held by insiders.
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- Clinical Research Advancement: Fennec Pharmaceuticals will present four independent studies at the 2026 American Society of Clinical Oncology Annual Meeting, aimed at evaluating the application of PEDMARK® across diverse patient populations, further validating its clinical utility in adolescent and adult patients to address significant unmet medical needs.
- Significant Hearing Protection Effects: The STS-J01 study from the Japanese Children's Cancer Group demonstrated that among 27 patients aged 3-18 receiving PEDMARK®, the incidence of hearing loss was significantly reduced to 16-24%, compared to 56-63% in the control group, indicating PEDMARK®'s effectiveness in reducing chemotherapy-related hearing loss.
- Applicability in Adult Patients: A retrospective case series involving young adults aged 18-39 showed that PEDMARK® can be safely integrated with cisplatin without compromising its antitumor activity, demonstrating its feasibility in adult oncology workflows.
- Strategic Importance: Fennec Pharmaceuticals' research underscores the significance of PEDMARK® in cancer treatment and reflects the company's long-term commitment to improving patient quality of life, thereby enhancing focus on hearing protection post-chemotherapy.
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- Stock Option Grant: On May 11, 2026, Fennec Pharmaceuticals approved the grant of 50,000 stock options to three new non-executive employees, aimed at attracting talent and enhancing the company's competitive edge.
- Option Details: The granted stock options consist of 49,141 incentive stock options and 859 nonqualified stock options, with an exercise price of $9.75 per share, reflecting the closing price on March 15, 2026, and a ten-year term.
- Vesting Schedule: One-third of each stock option will vest on the one-year anniversary of the grant date, with monthly vesting thereafter over 24 months, designed to incentivize long-term employee retention and improve productivity.
- Market Strategy: Fennec focuses on the commercialization of PEDMARK® to reduce the risk of ototoxicity in cancer patients, and the exclusive licensing agreement with Norgine is expected to further expand market coverage and strengthen the company's position in the global pharmaceutical market.
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- Earnings Beat: Fennec Pharmaceuticals reported a Q1 GAAP EPS of $0.01, exceeding expectations by $0.04, indicating improved profitability and boosting investor confidence.
- Significant Revenue Growth: The company achieved revenues of $15.11 million in Q1, a 72.7% year-over-year increase, surpassing market expectations by $1.27 million, demonstrating strong demand for its PEDMARK® product.
- Strong Cash Position: As of March 31, 2026, Fennec's cash and cash equivalents stood at $40.1 million, up from $36.8 million as of December 31, 2025, reflecting effective cash management.
- Positive Future Outlook: The company anticipates that its cash, cash equivalents, and investment securities as of March 31, 2026, will be sufficient to fund its business based on the current operating plan, showcasing management's confidence in future revenues.
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- Earnings Release Schedule: Fennec Pharmaceuticals plans to release its Q1 2026 financial results before the U.S. market opens on May 14, 2026, with management hosting a conference call and webcast to discuss financial and business outcomes, which is expected to positively impact investor confidence.
- Call Timing and Links: The conference call is scheduled for 8:30 a.m. Eastern Time on May 14, and investors can access the live webcast link via the company’s website, ensuring connection at least 15 minutes prior to avoid technical issues, demonstrating the company's commitment to transparency and investor communication.
- PEDMARK® Commercialization Progress: Fennec focuses on the commercialization of PEDMARK® to reduce the risk of ototoxicity in cancer patients receiving cisplatin-based chemotherapy, with FDA approval in 2022 and subsequent approvals in Europe and the U.K. in 2023, marking a strategic positioning in the oncology market.
- Exclusive Licensing Agreement: In March 2024, Fennec entered into an exclusive licensing agreement with Norgine Pharmaceuticals to commercialize PEDMARQSI® in Europe, the U.K., Australia, and New Zealand, which will further enhance Fennec's international market presence and sales potential.
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