Ascelia Pharma AB (publ) (STO:ACE)

Sweden flag Sweden · Delayed Price · Currency is SEK
2.960
-0.065 (-2.15%)
Apr 28, 2026, 5:29 PM CET
-6.62%
Market Cap 383.78M
Revenue (ttm) n/a
Net Income (ttm) -76.25M
Shares Out 126.87M
EPS (ttm) -0.67
PE Ratio n/a
Forward PE 11.86
Dividend n/a
Ex-Dividend Date n/a
Volume 515,713
Average Volume 843,930
Open 3.060
Previous Close 3.025
Day's Range 2.950 - 3.115
52-Week Range 2.530 - 5.230
Beta 0.87
RSI 47.59
Earnings Date May 12, 2026

About Ascelia Pharma AB

Ascelia Pharma AB (publ), a biotech company, develops identifies, develops, and commercializes novel drugs to treat orphan oncology treatments in Sweden. It develops Orviglance, a novel non-gadolinium diagnostic drug, which is in Phase 3 clinical trial for use in MRI-scans of the liver; and Oncoral, a novel oral irinotecan chemotherapy tablet, that is in Phase 2 clinical trial for the treatment of gastric cancer. The company has a collaboration agreement with the Taiho Oncology Inc. Ascelia Pharma AB (publ) was incorporated in 1999 and is headq... [Read more]

Industry Biotechnology
Sector Healthcare
Founded 1999
Employees 10
Stock Exchange Nasdaq Stockholm
Ticker Symbol ACE
Full Company Profile

Financial Performance

Financial Statements

News

Ascelia Pharma AB Transcript: DNB Carnegie Healthcare Seminar 2026

Orviglance, a manganese-based liver MRI agent for patients with severe renal disease, is under FDA review with a July 3 PDUFA date and strong Phase 3 data. Commercialization will rely on partnerships, and the company is also advancing Oncoral, an oral irinotecan, into further development.

7 weeks ago - Transcripts

Ascelia Pharma AB (FRA:7ZA) Q4 2025 Earnings Call Highlights: FDA Review Progress and Strategic ...

Ascelia Pharma AB (FRA:7ZA) Q4 2025 Earnings Call Highlights: FDA Review Progress and Strategic Challenges

2 months ago - GuruFocus

Q4 2025 Ascelia Pharma AB Earnings Call Transcript

Q4 2025 Ascelia Pharma AB Earnings Call Transcript

2 months ago - GuruFocus

Ascelia Pharma AB Earnings Call Transcript: Q4 2025

Lead program Orviglance is in FDA review with a decision expected by July, targeting a significant unmet need in liver imaging for cancer patients with severe renal impairment. Financials show a SEK 16 million Q4 loss and SEK 50 million cash, with partnership discussions and launch preparations progressing well.

2 months ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q4 2025

Orviglance is on track for FDA approval in July 2026, targeting an $800M global market for liver MRI contrast in cancer patients with severe kidney impairment. Q4 saw a SEK 16M operating loss, SEK 15M in liquid assets, and ongoing partnering discussions for commercialization.

2 months ago - Transcripts

Ascelia Pharma AB Transcript: ABGSC Investor Days

The company is advancing Orviglance, a gadolinium-free liver MRI agent for patients with severe renal impairment, with FDA approval expected by July 3rd. Extensive clinical data and strong market research support its differentiation and commercial potential, while partner discussions and medical community engagement are ongoing.

5 months ago - Transcripts

Ascelia Pharma AB Transcript: DNB Carnegie Småbolagsdag

A novel manganese-based imaging agent for liver cancer is nearing FDA approval, offering a safer alternative to gadolinium for patients with kidney issues. Clinical trials show improved detection of small lesions and a strong safety profile, with commercialization plans underway.

5 months ago - Transcripts

Ascelia Pharma AB (FRA:7ZA) Q3 2025 Earnings Call Highlights: Strategic Advances and Financial ...

Ascelia Pharma AB (FRA:7ZA) Q3 2025 Earnings Call Highlights: Strategic Advances and Financial Strength

6 months ago - GuruFocus

Q3 2025 Ascelia Pharma AB Earnings Call Transcript

Q3 2025 Ascelia Pharma AB Earnings Call Transcript

6 months ago - GuruFocus

Ascelia Pharma AB Earnings Call Transcript: Q3 2025

NDA for Orviglance submitted, targeting FDA approval for liver MRI in high-risk patients. SEK 30M raised and convertibles converted, extending runway into Q4 next year. Focus remains on securing a commercialization partner and preparing for a U.S. launch.

6 months ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q3 2025

OrbiGlans NDA was submitted to the FDA, with approval expected by July 2026, targeting a $800M market for liver imaging in cancer patients with impaired kidney function. Financials show a SEK 15M Q3 loss, SEK 72M in cash, and a strengthened balance sheet after recent financing.

6 months ago - Transcripts

Ascelia Pharma AB (FRA:7ZA) Q2 2025 Earnings Call Highlights: Strategic Moves and Market ...

Ascelia Pharma AB (FRA:7ZA) Q2 2025 Earnings Call Highlights: Strategic Moves and Market Potential for Orviglance

8 months ago - GuruFocus

Q2 2025 Ascelia Pharma AB Earnings Call Transcript

Q2 2025 Ascelia Pharma AB Earnings Call Transcript

8 months ago - GuruFocus

Ascelia Pharma AB Earnings Call Transcript: Q2 2025

NDA submission for Orviglance is imminent, with strong clinical results and a clear commercialization strategy focused on partnering. Financial position is stable through year-end, supported by recent warrant proceeds and loan repayment.

8 months ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q2 2025

NDA submission for Orviglance is imminent, supported by strong clinical data and robust financials, with SEK 60 million in cash and a clear commercialization strategy focused on partnerships. Oncoral's phase II start depends on securing sufficient partnering funds.

8 months ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q1 2025

Orviglance is advancing toward FDA submission in early August, supported by strong phase 3 data and a recent SEK 43 million warrant exercise, extending the cash runway to year-end. Partnering discussions are ongoing, with a focus on optimizing commercialization and financial sustainability.

1 year ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q1 2025

Orviglance is on track for NDA submission in August 2025, supported by strong phase III data and a robust financial position after a successful warrant exercise. Partnering discussions for commercialization are advancing, with the U.S. prioritized for launch.

1 year ago - Transcripts

Ascelia Pharma AB Transcript: ABGSC Investor Days

Orviglance, a manganese-based MRI agent for patients with severe renal disease, is on track for NDA submission mid-year after strong phase III results. Commercialization will be through a partner, targeting a focused U.S. market segment, while industry trends favor safer, non-gadolinium agents.

1 year ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q4 2024

Orviglance completed phase III with strong results and is on track for NDA submission mid-2025, targeting a significant unmet need in liver imaging for cancer patients with kidney impairment. Financials show a Q4 loss and a solid cash runway, with commercialization and partnering progressing.

1 year ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q3 2024

Orviglance achieved positive phase III results and is advancing toward NDA submission, supported by a fully subscribed SEK 105M rights issue that extends the cash runway to late 2025. Commercialization and partnering discussions are ongoing, with Oncoral set for phase II in gastric cancer.

1 year ago - Transcripts

Ascelia Pharma AB Earnings Call Transcript: Q2 2024

Strong Phase 3 results for Orviglance set the stage for NDA submission and commercialization, supported by a SEK 105 million rights issue. Q2 saw reduced losses and ongoing partnering discussions, with a focus on regulatory milestones and launch readiness.

1 year ago - Transcripts

Ascelia Pharma AB Transcript: HC Andersen Life Science Seminar

The presentation highlighted strong phase III results for Orviglance, a novel oral diagnostic for cancer patients with renal disease, with NDA submission targeted for mid-2025. Commercialization efforts focus on the U.S. market, while Oncoral's development will proceed as resources allow.

2 years ago - Transcripts