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AC Immune First Quarter 2026 Financial and Corporate Updates

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(Moderate)
Rhea-AI Sentiment
(Positive)
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AC Immune (NASDAQ: ACIU) reported Q1 2026 corporate and clinical updates and cash resources of CHF 74.8 million as of March 31, 2026, providing runway into Q4 2027. Key program moves: dosing started in Phase 1 of the brain-penetrant NLRP3 inhibitor ACI-19764, final ABATE cohort AD4 initiated (triggers $12M payment), and an amended Morphomer Tau deal with Lilly includes a CHF 10M upfront payment.

Anticipated 2026 readouts include ABATE 12-month interim data (H1), Part 1 VacSYn final data (H2), and Phase 1 ACI-19764 results (H2).

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AI-generated analysis. Not financial advice.

Positive

  • Cash runway into Q4 2027 with CHF 74.8 million total cash resources
  • $12 million milestone triggered by treatment of first AD4 patient in ABATE
  • CHF 10 million upfront payment from amended Morphomer-Tau collaboration with Lilly
  • Net loss narrowed to CHF 14.8 million from CHF 19.0 million year-ago period
  • Dosed first subjects in Phase 1 for brain-penetrant ACI-19764

Negative

  • Total cash resources declined from CHF 91.4M (Dec 31, 2025) to CHF 74.8M (Mar 31, 2026)
  • Enrollment paused in partner-run ReTain (JNJ-2056) study, limiting near-term data accrual
  • R&D spend decreased to CHF 11.8M from CHF 15.9M, reflecting cost cuts that may affect program pacing

News Market Reaction – ACIU

+3.41%
2 alerts
+3.41% News Effect
+$10M Valuation Impact
$318.04M Market Cap
0.0x Rel. Volume

On the day this news was published, ACIU gained 3.41%, reflecting a moderate positive market reaction. Our momentum scanner triggered 2 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $10M to the company's valuation, bringing the market cap to $318.04M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Cash resources: CHF 74.8 million Cash & equivalents: CHF 19.2 million Short-term financial assets: CHF 55.6 million +5 more
8 metrics
Cash resources CHF 74.8 million As of March 31, 2026; funding into Q4 2027
Cash & equivalents CHF 19.2 million Component of Q1 2026 cash resources
Short-term financial assets CHF 55.6 million Component of Q1 2026 cash resources
Q1 2026 R&D expenses CHF 11.8 million Versus CHF 15.9 million in Q1 2025
Q1 2026 G&A expenses CHF 4.2 million Versus CHF 4.4 million in Q1 2025
Net loss Q1 2026 CHF 14.8 million Versus CHF 19.0 million in Q1 2025
Takeda milestone $12 million Triggered by first patient treated in AD4 cohort
Lilly upfront payment CHF 10 million Amended Morphomer Tau collaboration (Q2 2026 event)

Market Reality Check

Price: $2.19 Vol: Volume 173,273 is below t...
low vol
$2.19 Last Close
Volume Volume 173,273 is below the 20-day average of 267,047 (relative volume 0.65x). low
Technical Trading near its 200-day MA, with price at 2.93 versus 200-day MA of 2.89.

Peers on Argus

ACIU fell 3.3% while several biotech peers like EDIT (-6.47%), SLN (-7.66%), VYG...

ACIU fell 3.3% while several biotech peers like EDIT (-6.47%), SLN (-7.66%), VYGR (-2.93%), and IMMP (-2.33%) were also down; PRQR rose 1.32%. No peers appeared in the momentum scanner, suggesting a stock-specific rather than coordinated sector move.

Previous Earnings Reports

5 past events · Latest: Mar 13 (Neutral)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 13 Full-year 2025 results Neutral +0.5% Reported FY 2025 loss and cash of CHF 91.4M with pipeline updates.
Nov 04 Q3 2025 results Positive +3.8% Q3 2025 update with CHF 108.5M cash and narrowed R&D focus.
Aug 05 Q2 2025 results Positive +11.6% Q2 2025 results with CHF 127.1M cash and positive VacSYn data.
Apr 30 Q1 2025 results Positive +1.8% Q1 2025 update showing strong Phase 2 ACI-7104 data and cash of CHF 145.7M.
Mar 13 Full-year 2024 results Positive -0.9% FY 2024 results featuring large Takeda deal and CHF 165.5M cash.
Pattern Detected

Earnings and corporate updates have typically seen modestly positive or muted reactions, with one notable negative divergence despite seemingly constructive news.

Recent Company History

Across prior earnings and results updates, AC Immune consistently highlighted strong cash resources and advancing neurodegenerative programs. Cash ranged from CHF 165.5M in full-year 2024 to CHF 91.4M at year-end 2025, with funding guidance generally into Q1–Q3 2027. Market reactions to these earnings events were usually small single‑digit moves around neutral to positive territory. Today’s Q1 2026 update, with cash of CHF 74.8M and reduced quarterly loss of CHF 14.8M, fits the pattern of pairing financial stewardship with pipeline progress.

Historical Comparison

+3.4% avg move · In the last five earnings-style releases, ACIU’s average move was about 3.36%, generally modestly po...
earnings
+3.4%
Average Historical Move earnings

In the last five earnings-style releases, ACIU’s average move was about 3.36%, generally modestly positive. A current move of -3.3% after this Q1 2026 update would contrast with that typical reaction profile.

Earnings updates have shown cash declining from CHF 165.5M in FY 2024 to CHF 74.8M in Q1 2026, while funding guidance remains into 2027 and clinical programs like ACI‑7104, ACI‑24.060, and ACI‑19764 advance through Phase 2 and Phase 1 milestones.

Market Pulse Summary

This announcement combined Q1 2026 financials with multiple clinical milestones, including Phase 1 p...
Analysis

This announcement combined Q1 2026 financials with multiple clinical milestones, including Phase 1 progress for ACI‑19764 and advancing Phase 2 programs ACI‑7104 and ACI‑24.060. Cash resources of CHF 74.8M are expected to fund operations into Q4 2027, while R&D and G&A expenses declined versus 2025. Investors may track upcoming 2026 readouts, collaboration payments like the $12M Takeda milestone and CHF 10M Lilly upfront, and how these influence future loss levels and runway.

Key Terms

phase 1, phase 2, nlrp3 inflammasome, p-tau, +4 more
8 terms
phase 1 medical
"Dosed first subjects in Phase 1 trial of brain-penetrant small molecule"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
phase 2 medical
"Final data from Part 1 of the Phase 2 VacSYn trial in PD | H2 2026"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
nlrp3 inflammasome medical
"targeting the NLRP3 inflammasome.Morphomer NLRP3 inhibitors have potential"
A protein complex inside immune cells that acts like a cellular smoke alarm: it senses stress or danger signals and triggers a rapid inflammatory response by activating enzymes that release inflammatory molecules. Investors pay attention because blocking or modulating this pathway is a major drug-development target for a range of diseases (inflammatory, cardiovascular, metabolic, neurodegenerative), so progress, trial results, safety signals, or regulatory decisions around NLRP3-targeting therapies can materially affect clinical prospects, market size, and company valuation.
p-tau medical
"ACI-35 (JNJ-2056) anti-pTau active immunotherapy AC Immune’s partner"
p‑tau is a form of the brain protein tau that has had phosphate chemical tags attached, a change linked to the abnormal clumping and breakdown of nerve cells in diseases like Alzheimer’s. It matters to investors because measuring p‑tau in spinal fluid or blood acts like an early smoke detector for neurodegeneration and is used to select patients, track drug effect, and influence the commercial value of diagnostics and treatments in the neurological disease market.
tdp-43 medical
"first in vivo images of TDP-43 pathology in the human brain, detected"
TDP-43 is a protein inside cells that helps regulate how genetic instructions are used; when it misfolds or accumulates into clumps in brain or spinal cord cells, it is linked to neurodegenerative conditions like ALS and some dementias. For investors, TDP-43 matters because it is a clear biological target for diagnostics and therapies—detecting or stopping its abnormal behavior could change patient care and create commercial value, similar to fixing a faulty part in a complex machine.
positron emission tomography medical
"first-in-class positron emission tomography (PET) tracer ACI-19626, at"
A positron emission tomography (PET) scan is an imaging test that uses a tiny amount of radioactive tracer injected into the body to map how organs and tissues are functioning, similar to watching traffic flow on a city map rather than just seeing roads. Investors care because PET technology and the tracers it uses are critical in developing and measuring the effectiveness of drugs, diagnosing diseases, and guiding treatment decisions, which can drive demand, regulatory scrutiny, and revenue for related healthcare companies.
pet tracer medical
"first-in-class positron emission tomography (PET) tracer ACI-19626, at"
A PET tracer is a tiny, short‑lived radioactive molecule given to a patient that acts like a fluorescent tag inside the body so a PET (positron emission tomography) scanner can reveal where specific cells or chemicals are active. Investors care because tracers enable diagnostics, guide and speed drug development, and create commercial and regulatory value through hospital use, imaging centers, intellectual property and reimbursement — similar to how a new sensor can unlock new features and revenue for a tech device.
ind-enabling studies regulatory
"Investigational New Drug (IND)-enabling studies are expected to be initiated"
Ind-enabling studies are early research efforts that test whether a new drug or treatment is safe and effective enough to move forward in development. They are like preliminary tests to ensure a product works as intended before investing more resources into large-scale trials. For investors, these studies are important because successful results can signal potential progress toward bringing a new product to market, impacting its future value.

AI-generated analysis. Not financial advice.

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AC Immune First Quarter 2026 Financial and Corporate Updates

  • Dosed first subjects in Phase 1 trial of brain-penetrant small molecule NLRP3 inhibitor ACI-19764 with SAD/MAD results in healthy volunteers expected in H2 2026
  • Initiated final cohort, AD4, in ABATE Phase 1b/2 trial of ACI-24 to treat Alzheimer's Disease triggers milestone payment, as announced separately today
  • Amended Morphomer® Tau collaboration with Lilly reflects growing excitement for targeting intracellular Tau and significant progress with our Morphomer® small molecules
  • Approaching multiple milestones including 12-month interim results of the AD3 cohort in ABATE in Q2 2026 and full data from Part 1 of ACI-7104 VacSYn Phase 2 trial expected in H2 2026
  • Cash resources of CHF 74.8 million as of March 31, 2026, provide funding into Q4 2027

Lausanne, Switzerland, April 30, 2026 -- AC Immune SA (NASDAQ: ACIU), a clinical-stage biopharmaceutical company pioneering precision therapeutics for neurodegenerative diseases, today provided financial and corporate updates for the quarter ended March 31, 2026.

Dr. Andrea Pfeifer, CEO of AC Immune SA, commented: “The progress in our collaborations with Takeda and Eli Lilly reflect great confidence in our anti-Abeta active immunotherapy and Tau aggregation inhibitor small molecules, respectively. These have the potential to change the way we target the proteinopathies that drive Alzheimer’s and other neurodegenerative diseases (NDDs). This is further exemplified by the presentation of the interim results for ACI-7104 at AD/PD 2026 showing that our active immunotherapy targeting a-synuclein (a-syn) has the potential to modify disease pathology in Parkinson’s disease (PD). We also advanced our NLRP3 inhibitor ACI-19764 into clinical development, further demonstrating the power of AC Immune’s technology to target the key pathways that contribute to neurodegeneration.

“We are now moving towards multiple value inflection points during 2026. These include Phase 2 data readouts on our active immunotherapies ACI-7104 and ACI-24, and initial results from the Phase 1 trial of ACI-19764 also anticipated this year.”

Q1 2026 and Subsequent Highlights:

ACI-24 anti-Abeta active immunotherapy

  • As announced separately today, AC Immune has initiated the final cohort, AD4, in the ongoing Phase 1b/2 ABATE trial of ACI-24 to treat Alzheimer's Disease
  • Treatment of the first patient in cohort AD4 triggers a $12 million milestone payment from Takeda

Morphomer-Tau small molecule program

  • Amended agreement with Eli Lilly and Co. (Lilly) reflects growing excitement for targeting intracellular Tau and significant progress with our Morphomer small molecules
  • The amendment continues the research and collaboration to cover development of new lead Tau Morphomer® candidates and potential back-up compounds.
  • Under this amendment, AC Immune receives a CHF10 million upfront payment (Q2 2026 event) and a subsequent milestone payment subject to Phase 1 dosing, in addition to milestones announced in a prior amendment. AC Immune is eligible for further development, regulatory and commercial milestones of over CHF1.7 billion, plus tiered percentage royalty payments in the low double digits, as previously disclosed.
  • Investigational New Drug (IND)-enabling studies are expected to be initiated imminently.

ACI-7104, anti-a-syn active immunotherapy

  • Presented updated interim results from Part 1 of the Phase 2 VacSYn clinical trial in early-stage Parkinson's disease at the International Conference on Alzheimer’s and Parkinson’s Diseases (AD/PD™ 2026), including promising biomarker data.
    • Interim results previously presented include changes in biomarkers and clinical measures all suggesting potential disease modification through treatment with ACI-7104
    • Final results for the week 104 full data set from Part 1 of the VacSYn trial expected to be reported in H2 2026.

NLRP3 inhibitor, ACI-19764, small molecule program

  • Dosed the first subjects in a Phase 1 clinical trial of ACI-19764, a brain-penetrant Morphomer small molecule targeting the NLRP3 inflammasome.
  • Morphomer NLRP3 inhibitors have potential to intervene at the earliest stages of disease in neurodegenerative conditions, including AD, PD, amyotrophic lateral sclerosis (ALS) and frontotemporal dementia.
  • Potential additional indications include inflammatory disorders, cardiovascular disease, metabolic disorders, skin inflammatory diseases, and certain rare diseases, among others.

ACI-35 (JNJ-2056) anti-pTau active immunotherapy

  • AC Immune’s partner Janssen Pharmaceuticals, Inc. (Janssen), a Johnson & Johnson company, is seeking a protocol amendment for the ReTain study to enable earlier insights into the biological activity of JNJ-2056 and its potential for clinical benefit. Submissions to all relevant health authorities are ongoing.
  • The study remains active, with enrollment paused, and there is no change for enrolled participants at this time.
  • The study is ongoing based on ~60 enrolled patients with a minimum of 12 months and up to 24 months of treatment and follow-up.

TDP-43 PET tracer

  • Presented Phase 1 data including the first in vivo images of TDP-43 pathology in the human brain, detected using its first-in-class positron emission tomography (PET) tracer ACI-19626, at the International Conference on Alzheimer’s and Parkinson’s Disease (AD/PD™ 2026).
  • Initial Phase 1 data (PET scans) with ACI-19626 showed that tracer uptake was significantly higher in key regions of the brain in patients with frontotemporal dementia (FTD) and we are currently evaluating the tracer in ALS patients.
  • Clinical data indicate a pharmacokinetic (PK) profile suitable for human brain imaging and potentially pharmacodynamic analysis of therapeutics targeting TDP-43 pathology.

AC Immune AD/PDTM 2026 symposium

  • Hosted an industry symposium on achieving precision prevention in Parkinson’s disease, highlighting Phase 2 clinical data on our ACI-7104 active immunotherapy, our small molecule programs targeting intracellular alpha-synuclein, and innovative diagnostic approaches to identifying at-risk individuals.

Anticipated 2026 Milestones

ProgramMilestoneExpected in
ACI-7104.056
anti-a-syn active immunotherapy
Final data from Part 1 of the Phase 2 VacSYn trial in PDH2 2026
ACI-24.060
anti-Abeta active immunotherapy
Interim results from ABATE Phase 2 trial after reaching 12-month treatment timepoint in the AD3 cohortH1 2026
ACI-19764
NLRP3 inhibitor
Results from Phase 1 trial in healthy volunteersH2 2026
Morphomer-Tau aggregation inhibitorsInitiation of IND-enabling studiesH1 2026
Morphomer a-syn aggregation inhibitorLead declarationH1 2026


Analysis of Financial Statements for the Quarter Ended March 31, 2026

  • Cash Position: The Company had total cash resources of CHF 74.8 million (CHF 91.4 million as of December 31, 2025), composed of CHF 19.2 million in cash and cash equivalents and CHF 55.6 million in short-term financial assets. The Company’s cash resources are expected to provide sufficient capital to last into Q4 2027, excluding potential milestone payments.
  • R&D expenditures: R&D expenses for the three months ended March 31, 2026, were CHF 11.8 million, compared with CHF 15.9 million for the comparable period in 2025. The decrease was partly due to lower personnel and operational spend of approximately CHF 1.7 million as a result of our pipeline focus initiatives announced in Q3 2025, as well as lower spend associated with our active immunotherapy programs, particularly in the upfront CMC costs prior to initiation of phase 2 studies.
  • G&A expenditures: G&A expenses in the period were CHF 4.2 million in the period ended March 31, 2026, compared to CHF 4.4 million for same period in 2025.
  • Financial result: The financial result was a loss of less than CHF 0.1 million for the period, compared with a gain of CHF 0.3 million for the comparable period. The change was primarily driven by a decrease in interest income earned on short-term financial assets, partially offset by lower foreign exchange losses.
  • IFRS loss for the period: The Company had a net loss of CHF 14.8 million for the period ended March 31, 2026, compared to CHF 19.0 million for the same period in 2025.

About AC Immune SA 

AC Immune SA is a clinical-stage biopharmaceutical company and a global leader in precision prevention for neurodegenerative diseases, including Alzheimer’s disease, Parkinson’s disease, and NeuroOrphan indications driven by misfolded proteins. The Company’s two clinically validated technology platforms, SupraAntigen® and Morphomer®, fuel its pipeline of first- and best-in-class assets, which currently features a range of therapeutic and diagnostic programs, including candidates in Phase 2 and Phase 3 development. AC Immune has a strong track record of securing strategic partnerships with leading global pharmaceutical companies, resulting in substantial non-dilutive funding to advance its proprietary programs and >$4.5 billion in potential milestone payments plus royalties.

SupraAntigen® is a registered trademark of AC Immune SA in the following territories: AU, EU, CH, GB, JP, RU, SG and USA. Morphomer® is a registered trademark of AC Immune SA in CA, CN, CH, EU, GB, JP, KR, NO, RU and SG.

The information on our website and any other websites referenced herein is expressly not incorporated by reference into, and does not constitute a part of, this press release.

For further information, please contact:

SVP, Investor Relations & Corporate Communications

Gary Waanders, Ph.D., MBA
AC Immune
Phone: +41 21 345 91 91
Email: gary.waanders@acimmune.com





 
International Media

Chris Maggos
Cohesion Bureau
Phone: +41 79 367 6254
Email: chris.maggos@cohesionbureau.com
 

Forward looking statements

This press release contains statements that constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Forward-looking statements are statements other than historical fact and may include statements that address future operating, financial or business performance or AC Immune’s strategies or expectations. In some cases, you can identify these statements by forward-looking words such as “may,” “might,” “will,” “should,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “predicts,” “projects,” “potential,” “outlook” or “continue,” and other comparable terminology. Forward-looking statements are based on management’s current expectations and beliefs and involve significant risks and uncertainties that could cause actual results, developments and business decisions to differ materially from those contemplated by these statements. These risks and uncertainties include those described under the captions “Item 3. Key Information – Risk Factors” and “Item 5. Operating and Financial Review and Prospects” in AC Immune’s Annual Report on Form 20-F and other filings with the Securities and Exchange Commission. Forward-looking statements speak only as of the date they are made, and AC Immune does not undertake any obligation to update them in light of new information, future developments or otherwise, except as may be required under applicable law. All forward-looking statements are qualified in their entirety by this cautionary statement.

Condensed Consolidated Balance Sheets (Unaudited)
(In CHF thousands)

      
   As of
   March 31,  December 31, 
         2026    2025
Assets       
Non-current assets       
Property, plant and equipment  2,057 1,989
Right-of-use assets  4,310 4,540
Intangible asset  50,416 50,416
Long-term financial assets  585 584
Total non-current assets  57,368 57,529
      
Current assets     
Prepaid expenses  3,744 3,972
Accrued income  230 360
Other current receivables  1,282 978
Short-term financial assets  55,628 64,617
Cash and cash equivalents  19,169 26,795
Total current assets  80,053 96,722
Total assets   137,421 154,251
      
Shareholders' equity and liabilities     
      
Shareholders’ equity     
Share capital  2,257 2,253
Share premium  482,345 481,863
Treasury shares  (218) (218)
Currency translation differences  7 7
Accumulated losses  (452,857) (439,021)
Total shareholders’ equity  31,534 44,884
      
Non-current liabilities     
Long-term deferred contract revenue  1,292 2,339
Long-term lease liabilities  3,479 3,689
Net employee defined benefit liabilities  8,868 8,646
Total non-current liabilities  13,639 14,674
      
Current liabilities     
Trade and other payables  1,319 2,068
Accrued expenses  6,469 8,067
Short-term deferred contract revenue  83,635 83,706
Short-term lease liabilities  825 852
Total current liabilities  92,248 94,693
Total liabilities  105,887 109,367
Total shareholders’ equity and liabilities  137,421 154,251


Condensed Consolidated Statements of Income/(Loss) (Unaudited)
(In CHF thousands, except for per-share data)

      
   For the Three Months
   Ended March 31, 
   2026 2025
Revenue                
Contract revenue  1,119 990
Total revenue  1,119 990
      
Operating expenses     
Research & development expenses  (11,744) (15,916)
General & administrative expenses  (4,174) (4,443)
Other operating income/(expense), net  11 (1)
Total operating expenses  (15,907) (20,360)
Operating loss  (14,788) (19,370)
      
Financial income  228 687
Financial expense  (65) (54)
Exchange differences  (176) (292)
Finance result, net  (13) 341
      
Loss before tax  (14,801) (19,029)
Income tax expense   
Loss for the period  (14,801) (19,029)
      
Loss per share:     
Basic and diluted loss per share for the period attributable to equity holders  (0.15) (0.19)


Condensed Consolidated Statements of Comprehensive Income/(Loss) (Unaudited)
(In CHF thousands)

      
   For the Three Months
   ended March 31, 
         2026    2025
Loss for the period  (14,801) (19,029)
Items that will be reclassified to income or loss in subsequent periods (net of tax):     
Currency translation differences  0 4
Other comprehensive income/(loss)  0 4
Total comprehensive loss, net of tax   (14,801) (19,025)


Attachment


FAQ

What cash runway did AC Immune (ACIU) report on April 30, 2026?

AC Immune reported CHF 74.8 million in cash resources, providing funding into Q4 2027. According to AC Immune, this balance includes cash, cash equivalents and short-term financial assets and excludes potential future milestone receipts.

What milestone payments did AC Immune (ACIU) announce in Q1 2026?

Treatment of the first AD4 patient in ABATE triggered a $12 million payment; Lilly amendment includes a CHF 10 million upfront. According to AC Immune, additional development and regulatory milestones remain possible under existing agreements.

When are the next clinical readouts expected for AC Immune (ACIU) programs?

Key readouts: ABATE 12-month interim data in H1 2026 and VacSYn Part 1 final data in H2 2026. According to AC Immune, Phase 1 results for ACI-19764 are also expected in H2 2026.

What progress did AC Immune (ACIU) report on the NLRP3 inhibitor ACI-19764?

AC Immune dosed the first subjects in a Phase 1 trial of brain-penetrant ACI-19764. According to AC Immune, SAD/MAD results in healthy volunteers are expected in H2 2026.

How did AC Immune’s (ACIU) expenses change in Q1 2026 versus Q1 2025?

R&D expenses fell to CHF 11.8M from CHF 15.9M; G&A was CHF 4.2M versus CHF 4.4M. According to AC Immune, R&D decline partly reflects lower personnel and CMC spend tied to pipeline focus initiatives.