Highest-materiality recent filing
Fennec shareholders approve all proposals at 2026 annual meeting
All five director nominees elected: Islam, Rallis, Brughera, Cook, Hackman with ~20M+ votes each.
Fennec announces new PEDMARK data at ASCO showing hearing loss reduction in pediatric/AYA patients
Phase 2/3 STS-J01 study met primary endpoint: hearing loss 16-24% vs 56-63% historical control.
Fennec grants 50,000 stock options to three new employees as inducement awards
Options exercisable at $9.75/share, 10-year term, vest over 3 years (1/3 on first anniversary, then monthly over 24 months).
Fennec board member Raykov retiring; board reduced to 5 directors
Rostislav Raykov notified company on Apr 27, 2026, of retirement from Board.
Fennec announces four PEDMARK abstracts accepted at 2026 ASCO meeting
Four abstracts evaluating PEDMARK accepted for presentation/publication at the 2026 ASCO Annual Meeting (May 29–June 2, Chicago).
Phase I/II study by University of Arizona Cancer Center to evaluate PEDMARK for preventing cisplatin-induced ototoxicity in head and neck and testicular cancer patients.
Fennec posts record FY2025 PEDMARK sales $44.6M (+50% YoY); Q4 $13.8M (+75%)
Full-year net product sales $44.6M vs $29.6M in 2024; Q4 $13.8M vs $7.9M in prior year.
Fennec settles PEDMARK patent litigation; Cipla barred from generic until 2033
Lawsuit dismissed; each party bears its own costs.
Fennec announces TGH Cancer Institute study of PEDMARK for ototoxicity in AYA and adult patients
Tampa General Hospital Cancer Institute initiates real-world study of PEDMARK (sodium thiosulfate) to reduce ototoxicity risk in AYA and adult patients receiving cisplatin.
Data from retrospective review of 15 adult HNC patients presented at 2026 MHNCS symposium (Feb 19-21).
Fennec announces City of Hope IST testing PEDMARK in adult testicular germ cell tumors
Phase I study (NCT07218913) evaluating PEDMARK to prevent cisplatin-induced ototoxicity in adults with stage II-III metastatic testicular germ cell tumors.
Primary endpoint met: hearing loss in 24% (ASHA) and 16% (Brock) of evaluable patients vs 56-63% historically.
Fennec Pharmaceuticals redeems all convertible notes, now debt-free
Redeemed all remaining Petrichor convertible notes for $21.73M (principal $19.48M, accrued interest $305k, redemption fee $1.95M).
Fennec raises $5.025M in Canadian private placement, redeems $21.7M Petrichor notes
Issued 670,000 common shares at US$7.50 per share for gross proceeds of $5,025,000 from existing institutional shareholders in Canada (excl. Quebec).
Fennec prices $35M public offering of 4.7M shares at $7.50/share to repay debt
Offering of 4,666,667 common shares at $7.50 per share; gross proceeds ~$35M.
All six director nominees elected; votes for each exceeded 13.2M versus under 1M withheld.
Fennec Pharma reports FY2024 PEDMARK sales $29.6M (+40% YoY); Q4 EBITDA loss $0.6M, cash $26.6M
FY2024 net product sales $29.6M, up 40% from $21.3M in 2023; net loss narrowed to $0.07M from $16.0M.
Fennec's partner Norgine launches PEDMARQSI in Germany for cisplatin-induced hearing loss prevention
PEDMARQSI (sodium thiosulfate injection) launched in Germany by Norgine for prevention of ototoxicity in pediatric patients.
Fennec repays $13M convertible debt; eliminates $1.5M annual interest
Repurchased and redeemed $13M of convertible notes on Dec 18, 2024; fully retires First and Third Closing Notes.
NICE issued positive final draft guidance recommending PEDMARQSI for prevention of cisplatin-induced hearing loss in patients aged 1 month-17 years with localized solid tumors.
Fennec Pharma appoints new CMO, CCO, CSO to accelerate growth
Pierre Sayad appointed CMO, Terry Evans CCO, Christiana Cioffi CSO, effective Oct. 28, 2024.
Fennec appoints Jeffrey Hackman as CEO, succeeding Rostislav Raykov
Hackman named CEO and director effective August 16, 2024; Raykov steps down after 15 years, remains on board.
Fennec COO Adrian Haigh departs; 66,667 options accelerated at $8.03
Adrian Haigh left COO role effective June 30, 2024; joined as COO Aug 2023 after nine years as independent director.
Fennec shareholders approve all proposals at 2024 annual meeting
Five director nominees elected: Khalid Islam, Rallis, Brughera, Cook, Raykov.
Fennec Pharma to report Q1 2024 results on May 14; conference call at 8:30am ET
First quarter 2024 financial results to be released before U.S. market open on Tuesday, May 14, 2024.
Fennec Pharma FY2023 PEDMARK sales $21.3M, Q4 net loss $2.7M; $43M licensing deal bolsters cash
FY2023 PEDMARK net product sales $21.3M (vs $1.5M in 2022); Q4 net sales $9.7M.
Fennec licenses PEDMARQSI to Norgine for EU/AU/NZ; €40M upfront, up to €210M milestones
Exclusive license covers Europe (incl. UK), Australia, New Zealand; Norgine to commercialize.
Fennec pre-announces Q4 2023 net revenue ~$9.2-9.7M, up 41-49% QoQ
Q4 2023 net revenue expected $9.2-9.7M, a 41-49% increase vs Q3 2023.
Fennec prelim Q4 2023 net revenue $9.2-9.7M (+41-49% QoQ); FY 2023 $20.7-21.2M
Q4 2023 net revenue expected $9.2-9.7M, up 41-49% from Q3 2023.
FDA reminds providers PEDMARK is not substitutable with other STS products
FDA publicly warned healthcare providers that PEDMARK (sodium thiosulfate injection) must not be substituted with other STS products.
Closed third tranche of $5M senior secured convertible notes under existing SPA with Petrichor.
Fennec Q3 2023: PEDMARK revenue $6.5M (+96% QoQ); UK approval for PEDMARQSI
PEDMARK net product revenue $6.5M in Q3 2023, up 96% from $3.3M in Q2 2023.
Fennec Q2 revenue $3.3M (+98% QoQ); appoints Adrian Haigh as COO
Net product revenue $3.3M in Q2 2023, up 98% from $1.7M in Q1 2023.
Fennec Q2 PEDMARK revenue $3.3M, up 98% QoQ; appoints Adrian Haigh as COO
Net product sales of PEDMARK $3.3M, a 98% sequential increase from Q1 2023.
Fennec Q2 revenue $3.3M (up 98% QoQ); appoints Adrian Haigh as COO
Net product sales of $3.3M for Q2 2023, up 98% from Q1 2023; gross profit $3.2M.
Fennec shareholders elect six directors, ratify auditor, approve say-on-pay at 2023 annual meeting
All six director nominees elected: Khalid Islam, Adrian Haigh, Chris A. Rallis, Marco Brughera, Jodi Cook, Rostislav Raykov.
Fennec gets EU approval for Pedmarqsi to prevent cisplatin-induced hearing loss in children
European Commission granted marketing authorization for Pedmarqsi (sodium thiosulfate) for pediatric localized solid tumors.
CHMP recommends EU marketing authorization for Pedmarqsi (sodium thiosulfate) to prevent ototoxicity in pediatric patients aged 1 month to <18 years with localized solid tumors.
Fennec receives FDA Orphan Drug Exclusivity for PEDMARK; 7-year market exclusivity until 2029
FDA granted Orphan Drug Exclusivity to PEDMARK, providing 7-year market exclusivity from Sept. 20, 2022 to Sept. 20, 2029.
NCCN AYA Oncology guidelines now recommend PEDMARK to reduce cisplatin-induced hearing loss in pediatric patients with localized, non-metastatic solid tumors.
Fennec launches PEDMARK in US for cisplatin-induced hearing loss in pediatric patients
PEDMARK is the first and only FDA-approved therapy to reduce cisplatin-induced ototoxicity in pediatric patients aged 1 month+ with localized solid tumors.
Fennec closes $20M second tranche of Petrichor notes triggered by FDA approval of PEDMARK
Second closing of $20M senior secured convertible notes funded after FDA approved PEDMARK on Sept 20, 2022.
FDA approved PEDMARK (sodium thiosulfate) for reducing ototoxicity in children aged 1 month+ with localized, non-metastatic solid tumors.
Fennec closes $5M initial tranche of $45M senior secured note; $20M on FDA approval of PEDMARK
First closing $5M senior secured note; $20M upon FDA approval of PEDMARK; up to $20M additional.
Fennec secures up to $45M from Petrichor; $5M now, $20M on FDA approval of PEDMARK
Petrichor invests $5M in convertible notes at $8.11/share; $20M additional due upon FDA approval of PEDMARK by Sep 30, 2022.
All six director nominees elected with >15.88M votes for each; broker non-votes of 5.3M on each.
Fennec resubmits NDA to FDA for PEDMARK to prevent pediatric ototoxicity
Resubmitted New Drug Application (NDA) for PEDMARK (sodium thiosulfate anhydrous injection).
Fennec Pharmaceuticals CCO Shubh Goel resigns; effective late February
Shubh Goel, chief commercial officer, tendered resignation on Jan 31, 2022.
Fennec amends loan agreement with Bridge Bank; sets PEDMARK NDA resubmission and approval milestones
Third Amendment to 2019 Loan & Security Agreement with Bridge Bank (Western Alliance Bank) dated Jan 27, 2022.
Fennec receives FDA Complete Response Letter for PEDMARK NDA citing manufacturing deficiencies
FDA issued CRL on Nov 29, 2021, after PDUFA date of Nov 27, citing manufacturing deficiencies for PEDMARK NDA.
On April 27, 2026, Rostislav Raykov notified Fennec Pharmaceuticals Inc. (the "Company") of his desire to retire from the Company's Board of Directors (the "Board") and that he will not stand for re-election at the Company's 2026 annual meeting of shareholders (the "Annual Meeting").
Ms. Christiana Cioffi, MBA, as Chief Strategy Officer ("CSO"),
On October 28, 2024, Fennec Pharmaceuticals Inc.'s (the "Company") announced the appointments of Mr. Pierre S. Sayad, PhD, M.S., as Chief Medical Officer ("CMO"),
Mr. Terry Evans as Chief Commercial Officer ("CCO"),
the Company announced the departure of Rostislav Raykov from his position as the Company’s Chief Executive Officer
the Company announced the appointment of Jeffrey S. Hackman as CEO and a member of the Board.
the Company announced the appointment of Jeffrey S. Hackman as CEO and a member of the Board.
On June 30, 2024, Adrian Haigh departed from his position as Fennec Pharmaceuticals Inc.’s (the "Company") Chief Operating Officer
Mr. Haigh had accepted the appointment as Chief Operating Officer.
Adrian Haigh had stepped down from the the position of Director of Fennec Pharmaceuticals Inc.
In the same press release it was announced that Mr. Haigh had accepted the appointment as Chief Commercial Officer.
Adrian Haigh had stepped down from the the position of Director of Fennec Pharmaceuticals Inc.
Max materiality 0.90 · Median 0.65 · Most common event other_material