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Medicus Pharma Ltd (MDCX) Q3 2026 Earnings Report

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MDCX Q3 2026 EPS Results

Actual EPS
-$11.64
Consensus EPS
-$5.91
Beat/Miss
Missed by -$5.73
One Year Ago EPS
-$56.00

MDCX Q3 2026 Revenue Results

Actual Revenue
$0
Expected Revenue
$0
Beat/Miss
Met expectations
YoY Revenue Growth
―

Earnings Announcement Details

Quarter
Q3 2026
Date
11/06/2026
Time
After Close
Conference Call
Friday, November 6, 2026
MDCX Upcoming Earnings

Medicus Pharma Ltd's next earnings date is estimated for March 26, 2027, based on past reporting schedules.

Q3 2026 Earnings Call Audio

MDCX Q3 2026 Earnings Call
0:00 / 0:00

Q3 2026 Earnings Slide Deck

No slide deck is available for this earnings event.

Q3 2026 Earnings Call Summary

Q3 2026
Earnings Call Date:Nov 06, 2026|% Change Since:-8.02%|
Earnings Call Sentiment|Positive

The call was predominantly positive, driven by the Pfizer collaboration, access to a clinical-stage ADC with prior development experience, a focused melanoma strategy, the proposed $135 million SkinJect business combination, continued Teverelix partnering efforts and new financing. Offsetting factors included a higher nine-month net loss and operating expense base, increased liabilities, limited unrestricted cash, pending clinical and regulatory milestones, manufacturing issues for Teverelix and uncertainty around the nonbinding SkinJect transaction.

Company Guidance

Medicus expects to concentrate incremental development investment on CD228V, initially in immunotherapy-resistant melanoma, with an objective response rate exceeding 30% as a development objective; it will advance SkinJect’s SKNJCT-005 study in parallel with the proposed business combination, targeting a $135 million pre-money enterprise valuation, concurrent equity financing, a projected estimate of approximately $3 million spread over the next 2 years, and completion during the first half of 2027, while management also described the budget as no more than $3 million spread over next 2 years; the company anticipates a substantial reduction in operating expenses in the coming quarters, expects FDA feedback on the Teverelix advanced prostate cancer program after approaching a 45-day mark, and said Teverelix product should become available sometime in the first quarter of next year.

  • Transformation into Precision Oncology Biotechnology CompanyDuring the first 9 months of 2026, Medicus advanced its transformation into a precision oncology-led biotechnology company and emphasized a capital-efficient drug development strategy, with incremental development investment prioritized toward CD228V.
  • Worldwide CD228V License and Pfizer CollaborationOn September 2, Medicus entered into a co-development and license agreement with Pfizer for CD228V, obtaining an exclusive worldwide license to develop, manufacture and commercialize the program, subject to retained rights and other provisions. Medicus has authority over program execution, while Pfizer remains involved in the co-development framework. Pfizer provided $2 million for development activities and retains the right, without an obligation, to elect to fund all or part of development beginning with the first pivotal trial.
  • Clinical-Stage ADC Asset with Existing Development FoundationCD228V is a second-generation antibody-drug conjugate originating from Seagen and subsequently advanced by Pfizer. Medicus stated that the program includes prior clinical, manufacturing and regulatory experience, including data from an open-label Phase I study of the predecessor SGN-CD228A that enrolled 88 patients with advanced solid tumors. Management also said Medicus has approximately 99 patients of data from the original Seagen study and 11 patients from Pfizer's CD228V program.
  • Established Vedotin Linker-Payload PlatformCD228V uses Pfizer's established vedotin linker-payload platform, with changes to the linker and the amount of payload carried by each antibody. Management stated that the technology has clinical and regulatory precedent through its use in FDA-approved ADC therapies.
  • Focused Melanoma Development StrategyMedicus's initial focus for CD228V is melanoma, particularly disease that has relapsed, become refractory or resisted immunotherapy. Management said the focused population is intended to address a substantial unmet need and guide future investment, rather than pursuing an unfocused pan-tumor development program.
  • Potential Meaningful Efficacy Benchmark for CD228VBased on the available clinical evidence for SGN-CD228A and the potential benefit of Pfizer's linker-payload reconstruction, management believes CD228V has the potential to achieve an objective response rate exceeding 30% in melanoma. The company stated that this remains to be demonstrated in clinical trials and would be subject to durable responses, an acceptable safety profile and applicable regulatory requirements.
  • Potential Expansion into Additional Tumor TypesManagement stated that, within the initial and subsequent studies, CD228V could be expanded into combinations with immunotherapy and other CD228-expressing tumor types, including squamous lung, esophageal and head and neck cancer.
  • SkinJect Business Combination ProposalSkinJect entered into a nonbinding letter of intent with an undisclosed SPAC. The proposed transaction contemplates a $135 million pre-money enterprise valuation for SkinJect, concurrent equity financing at closing, and Medicus seeking to retain majority economic and voting ownership of the combined company.
  • SkinJect Development Funding and Parallel AdvancementThe proposed SkinJect financing is intended to support the SKNJCT-005 study in Gorlin syndrome and preparation and submission of a potential new drug application. Management estimates approximately $3 million of spending over the next 2 years for the program and stated that Medicus will continue advancing SKNJCT-005 in parallel with the proposed transaction.
  • Teverelix Partnering OpportunitiesMedicus described Teverelix as offering partner-ready opportunities in acute urinary retention relapse prevention, advanced prostate cancer and women's health. The company is seeking global, regional or collaborative partners with the resources to advance these programs while maintaining program readiness.
  • Teverelix Study Design RefinementMedicus refined the acute urinary retention relapse-prevention study from an inherited 390-patient registrational-grade design to a 126-patient study. The company also submitted an advanced prostate cancer program design to the FDA and said it was approaching the 45-day mark for feedback.
  • Teverelix Manufacturing ProgressMedicus restarted Teverelix CMC work from scratch, is manufacturing the product and stated that the product should become available sometime in the first quarter of 2027.
  • Access to New CapitalDuring the 9 months ended September 30, 2026, Medicus raised approximately $42.5 million through equity and secured debt financing, net of issuance costs. After approximately $6.4 million of debt repayments, net cash provided by financing activities was $36.2 million.
  • Third-Quarter Expense and Net Loss ImprovementThird-quarter operating expenses were $14.5 million, compared with $15.4 million a year earlier, while third-quarter net loss was $15.2 million, compared with $16.0 million a year earlier.
  • Planned Operating Expense ReductionManagement stated that it anticipates a substantial reduction in operating expenses in the coming quarters and intends to align organizational costs with selected clinical, regulatory and strategic priorities.

MDCX Earnings History

MDCX earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Mar 26, 20272026 (Q4)-4.44--25.25――
Nov 06, 20262026 (Q3)-5.91-11.64-5679.21% (+44.36)
Aug 13, 20262026 (Q2)-6.38-10.50-21.551.16% (+11.00)
May 14, 20262026 (Q1)-9.60-15.50-2126.19% (+5.50)
Mar 25, 20262025 (Q4)-3.50-25.25-7-260.71% (-18.25)
Nov 14, 20252025 (Q3)-47.25-56.00-15.5-261.29% (-40.50)
Aug 12, 20252025 (Q2)-12.50-21.50-2514.00% (+3.50)
May 13, 20252025 (Q1)-12.33-21.00-8.03-161.52% (-12.97)
Mar 29, 20252024 (Q4)-13.70-7.00-15.3154.28% (+8.31)
Nov 23, 20242024 (Q3)-11.03-15.50-54.7971.71% (+39.29)

The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.

Beat Missed