Immunocore Holdings plc (IMCR) BCG Matrix

Immunocore Holdings plc (IMCR): BCG Matrix [Dec-2025 Updated]

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Immunocore Holdings plc (IMCR) BCG Matrix

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You're looking at Immunocore Holdings plc's portfolio, and honestly, it's the classic biotech story: one solid earner bankrolling a pipeline full of high-stakes potential. As of late 2025, KIMMTRAK, our main Cash Cow, is humming along, having pulled in $295.5 million in net product sales through the first nine months of the year, with growth still robust at 29% year-over-year. This revenue is the essential fuel for the promising Stars-like the expansion trials for tebentafusp and brenetafusp-and the big, risky Question Marks in autoimmune and infectious diseases. Let's break down exactly where Immunocore Holdings plc is placing its bets across the BCG Matrix to see what's driving value now and what could pay off big later.



Background of Immunocore Holdings plc (IMCR)

You're looking at a commercial-stage biotech, Immunocore Holdings plc, which focuses on developing immunotherapies across cancer, infectious diseases, and autoimmune conditions. They're known for their innovative TCR bispecific immunotherapies, built around their ImmTAX platform. Honestly, the company's current valuation is heavily tied to the success of its flagship product, KIMMTRAK, which treats unresectable or metastatic uveal melanoma in patients positive for the HLA-A02:01 allele. That's the core business right now.

Let's look at the numbers as of the third quarter of 2025. Immunocore Holdings plc posted net product sales of $103.7 million for Q3 2025, which was a solid 29% increase year-over-year. For the trailing twelve months ending September 30, 2025, total revenue hit $379.59 million, showing growth of 28.10% compared to the prior year. KIMMTRAK sales, specifically, grew 32% year-over-year for the first half of 2025. By the end of Q3 2025, KIMMTRAK was launched in 28 countries, continuing its global expansion efforts.

Financially, the company maintains a strong liquidity position; cash, cash equivalents, and marketable securities stood at $892 million as of September 30, 2025. Still, the focus on pipeline advancement means they're spending heavily-R&D expenses reached $70.6 million in Q3 2025, leading to a net loss of $0.2 million for that quarter. That spending is funding key late-stage oncology work, including the Phase 3 TEBE-AM trial, which is on track to complete enrollment in the first half of 2026, and the PRISM-MEL-301 trial, expecting dose selection in the second half of 2025.

Beyond melanoma, Immunocore Holdings plc is pushing its pipeline forward in other areas. They are advancing programs in oncology, like PRAME, and are also developing candidates for autoimmune diseases, such as Type 1 Diabetes, with a clinical trial application planned for late 2025. Plus, they were set to present initial Phase 1 data for their HBV (Hepatitis B virus) program in November 2025. The company is definitely balancing commercial execution with significant investment in future potential.



Immunocore Holdings plc (IMCR) - BCG Matrix: Stars

The Stars quadrant in the Boston Consulting Group Matrix represents Immunocore Holdings plc (IMCR) business units or products that possess a high market share within a high-growth market. For IMCR, the commercial success of KIMMTRAK (tebentafusp) and the aggressive clinical development of its pipeline assets into broader, high-potential melanoma indications firmly place them here. These assets are leaders but require substantial cash infusion to secure future market dominance, which is evident in the company's investment profile.

KIMMTRAK is the established leader, generating significant revenue while the company simultaneously invests heavily to expand its application into adjacent, high-growth segments. The overall Melanoma Therapeutics market is projected to be valued at $4.47 billion in 2025, indicating a high-growth environment for IMCR to defend and expand its position. The company's cash position of $892.4 million as of September 30, 2025, is being deployed to support this Star strategy, evidenced by Research & Development expenses reaching $70.6 million in the third quarter of 2025.

The Star category is defined by the current commercial success of KIMMTRAK and the near-term potential of its life-cycle management trials, which aim to capture additional market share in large patient populations. If these trials are successful, KIMMTRAK is positioned to transition into a Cash Cow as the growth rate of these expanded indications eventually slows.

The key components defining the Stars for Immunocore Holdings plc are:

  • KIMMTRAK is the standard of care in most launched markets.
  • Strong year-over-year net revenue growth for KIMMTRAK.
  • Phase 3 trials targeting large, previously untreated or adjuvant melanoma patient pools.
  • Significant investment in R&D to support these high-potential expansion indications.

Here is a look at the commercial performance of the core Star product, KIMMTRAK, and the associated pipeline expansion efforts as of the third quarter of 2025:

Metric Value/Status (as of Q3 2025) Context/Indication
KIMMTRAK Net Product Sales (Q3 2025) $103.7 million Metastatic Uveal Melanoma (mUM)
KIMMTRAK Net Product Sales (9M 2025) $295.5 million Metastatic Uveal Melanoma (mUM)
KIMMTRAK Quarterly Sales Growth (YoY) 29% Q3 2025 vs Q3 2024
KIMMTRAK Global Launches 28 countries mUM indication
TEBE-AM Phase 3 Enrollment Completion On track for 1H 2026 2L+ advanced cutaneous melanoma
PRISM-MEL-301 Phase 3 Dose Selection 160 mcg selected 1L advanced cutaneous melanoma (PRAME-positive)
ATOM Phase 3 Estimated Patient Population Up to 1,200 patients HLA-A02:01 high risk adjuvant uveal melanoma

Tebentafusp expansion into 2L+ advanced cutaneous melanoma (TEBE-AM Phase 3) represents a direct move to capture market share in a broader melanoma segment. The trial is on track to complete enrollment in the first half of 2026, which is a critical near-term milestone for this Star asset. This trial is consuming significant cash, as reflected in the $70.6 million R&D spend for the quarter, necessary to push this leader into a larger market.

Brenetafusp (IMC-F106C) in 1L cutaneous melanoma (PRISM-MEL-301 Phase 3) targets the large PRAME-positive market, which is a significant upside opportunity. The Independent Data Monitoring Committee review resulted in the selection of the 160 mcg dose as the go-forward dose, de-risking the registrational path. This move signals Immunocore Holdings plc's commitment to investing in its next-generation ImmTAC molecule to compete in the first-line setting.

The adjuvant uveal melanoma trial (ATOM Phase 3) for Kimmtrak is a significant market expansion for the existing Star product. The estimated HLA-A02:01 high risk adjuvant uveal melanoma patient population is up to 1,200 patients. Securing approval here would solidify KIMMTRAK's franchise potential by moving it into the earlier treatment setting, a classic Star strategy to convert a successful product into a long-term Cash Cow.

The company's overall pipeline assets targeting large, high-growth oncology markets are where the real upside is, as they leverage the validated ImmTAX platform. The cash position of $892.4 million as of September 30, 2025, is the fuel for these Star investments, even as the company reported a near break-even net loss of ($0.2) million for Q3 2025, which is a result of this high investment level.



Immunocore Holdings plc (IMCR) - BCG Matrix: Cash Cows

You're looking at the core engine of Immunocore Holdings plc's current financial strength, the product that generates more than it consumes. For Immunocore Holdings plc, that is definitely KIMMTRAK (tebentafusp), their approved, revenue-generating product for unresectable or metastatic uveal melanoma (mUM).

This product sits squarely in the Cash Cow quadrant because it holds a high market share in a mature, albeit rare, indication. KIMMTRAK continues to be the standard of care in most markets where it is launched. As of the third quarter of 2025, Immunocore Holdings plc has successfully launched KIMMTRAK in 28 countries globally, building on approvals in 39 countries.

The financial performance reflects this strong market position. For the first nine months of 2025, KIMMTRAK generated \$295.5 million in net product sales. This is a significant contribution, showing a 31% year-over-year sales growth for that nine-month period, which is what you want to see from a mature asset-it's still growing, just not at the explosive rate of a Star product.

Here's a quick look at the most recent quarterly sales performance, which drives the cash flow:

Metric Value (Q3 2025)
Net Product Sales (Q3 2025) \$103.7 million
Year-over-Year Sales Growth (Q3 2025) 29%
US Sales (Q3 2025) \$67.3 million
Europe Sales (Q3 2025) \$33.5 million
International Sales (Q3 2025) \$2.9 million

The growth story is compelling, showing the product is still expanding its reach. The 29% year-over-year growth in the third quarter of 2025 was fueled by global expansion and increasing treatment duration. Specifically, the US market saw 18% year-over-year quarterly sales growth, with the mean duration of treatment increasing to 14 months as of Q3 2025. Meanwhile, Europe and international regions combined saw a very robust 58% year-over-year quarterly sales growth, driven by new market launches.

This cash generation is exactly what you expect from a Cash Cow; it provides the capital to fund the rest of the business. Immunocore Holdings plc maintains a strong balance sheet to support its future. As of September 30, 2025, the company reported cash, cash equivalents, and marketable securities of \$892 million. This liquidity is critical for funding the R&D pipeline, which includes advancing three Phase 3 melanoma trials and multiple mid-stage programs.

You should view KIMMTRAK as the financial bedrock supporting Immunocore Holdings plc's ambitious pipeline development. The strategy here is to maintain that market leadership and efficiency, milking the gains passively while ensuring investments into supporting infrastructure-like global expansion and longer treatment durations-improve cash flow further. The key metrics supporting this Cash Cow status are:

  • Net product sales for nine months of 2025: \$295.5 million.
  • Cash balance as of Q3 2025: \$892 million.
  • KIMMTRAK launched in 28 countries globally.
  • Nine-month net product sales growth (YoY): 31%.
  • Q3 2025 net revenue growth (YoY): 29%.

Finance: draft the 13-week cash view incorporating the expected \$65 million sales-related rebate accruals for Q4 2025 by Friday.



Immunocore Holdings plc (IMCR) - BCG Matrix: Dogs

Dogs are business units or products with a low market share in low-growth markets. For Immunocore Holdings plc (IMCR), these represent pipeline elements or older assets that consume resources without offering clear, near-term commercial upside or significant strategic focus compared to the core KIMMTRAK franchise.

The allocation of resources to these lower-priority areas is reflected in the overall operating expenses. For the third quarter of 2025, Immunocore Holdings plc reported research and development expenses of $70.6 million, which reflects investment across the entire pipeline, including these less advanced or non-core efforts. Despite this spend, the company maintains a strong balance sheet, reporting $892 million in cash, cash equivalents, and marketable securities as of Q3 2025.

The category of Dogs can be identified by examining the trailing edge of the ImmTAX platform development:

  • Pre-clinical assets not yet prioritized for IND/CTA, consuming R&D spend without near-term milestones.
  • Older, non-core ImmTAX candidates that have not advanced beyond early Phase 1 trials.
  • Programs in therapeutic areas where the company lacks deep commercial or clinical expertise.
  • Any discontinued or shelved programs from the ImmTAX platform that failed early-stage proof-of-concept.

A concrete example of an early-stage program encountering a setback, which aligns with the Dog profile of failing early proof-of-concept, involves the brenetafusp (IMC-F106C) program. Specifically, one of the two dose regimens in the IMC-F106C-101 Phase 1/2 trial was discontinued following an initial review of the first 60 patients randomized in that specific experimental arm. Brenetafusp targets the PRAME (A02) antigen. While the overall brenetafusp program continues in Phase 3 for first-line advanced cutaneous melanoma, the discontinuation of a dose regimen in an early study is a classic indicator of a unit that did not meet expectations.

The company's expansion into infectious diseases and autoimmune conditions represents areas where commercial and clinical expertise is being built, contrasting with the established focus on oncology with KIMMTRAK. Programs in these newer areas, especially those still in pre-clinical stages or only recently entering early trials, carry a higher Dog-like risk profile until they demonstrate clear progression. For instance, the autoimmune candidate IMC-S118AI targeting Type 1 Diabetes has a target CTA/IND submission in 4Q 2025, and IMC-U120AI for Atopic Dermatitis is targeted for 2026. These represent cash consumption without the near-term revenue generation of the commercial product.

Here is a look at pipeline candidates that represent the lower-priority or higher-risk segments consuming R&D investment:

Program/Candidate Target Indication Area Latest Stage/Milestone (as of May 2025) Associated Financial Implication
Discontinued Dose Regimen of IMC-F106C Melanoma (PRAME) Discontinued after initial review of first 60 patients in Phase 1/2 trial Consumption of R&D spend without near-term return
IMC-I109V Hepatitis B Virus (HBV) / Infectious Disease Single Ascending Dose (SAD) Data expected in 2H 2025 Investment in non-core therapeutic area
IMC-S118AI Type 1 Diabetes / Autoimmune CTA/IND submission targeted for 4Q 2025 Cash consumption prior to potential IND filing
IMC-R117C Colorectal and GI cancers (PIWIL1) Phase 1/2 ongoing Early-stage clinical spend in a less advanced program

The management of these Dogs involves minimizing cash drain. The $70.6 million R&D expense in Q3 2025 must be scrutinized to ensure that spending on these lower-tier assets does not jeopardize the advancement of core assets like KIMMTRAK or the most promising Question Marks. You want to see clear, decisive action on these, as expensive turn-around plans rarely work in biotech R&D.



Immunocore Holdings plc (IMCR) - BCG Matrix: Question Marks

QUESTION MARKS (high growth products (brands), low market share): These are the programs where Immunocore Holdings plc is placing significant future bets, characterized by entry into large, growing therapeutic markets but currently possessing zero market share and high clinical risk.

The focus here is squarely on the pipeline candidates that have not yet achieved commercial success, consuming cash to fund their development. These units require heavy investment to move them toward Star status or risk them becoming Dogs if they fail to gain traction or prove efficacy.

The heavy investment required is clearly visible in the reported operating expenses. For the third quarter ended September 30, 2025, Research and development (R&D) expenses increased to $70.6 million, up from $52.8 million for the same period in 2024. This increase reflects the advancement of these high-risk, high-reward programs across oncology, infectious disease, and autoimmune areas.

The core Question Marks portfolio, as outlined, targets massive potential markets:

  • Autoimmune pipeline: IMC-S118AI (Type 1 Diabetes) and IMC-U120AI (Atopic Dermatitis).
  • Infectious disease candidates: IMC-M113V (HIV) and IMC-I109V (HBV).
  • Expansion oncology: Brenetafusp in non-melanoma solid tumors (e.g., ovarian cancer, NSCLC).

These programs are consuming capital from the commercial success of KIMMTRAK, which generated net product sales of $103.7 million in Q3 2025. The company maintained a cash position of $892 million as of September 30, 2025, to fund this necessary burn rate.

Here's a look at the status of these key Question Marks as of the latest reporting:

Candidate Therapeutic Area Target/Mechanism Key 2025/2026 Milestone
IMC-S118AI Autoimmune (Type 1 Diabetes) PPI (HLA-A02) x PD1 CTA/IND submission in 4Q 2025
IMC-U120AI Autoimmune (Atopic Dermatitis) CD1a (non-HLA restricted) x PD1 CTA/IND submission in 2026
IMC-M113V Infectious Disease (HIV) Gag (A02) Initial Phase 1 MAD data in Q1 2025
IMC-I109V Infectious Disease (HBV) Envelope (A02) SAD Data presentation in 2H 2025
Brenetafusp Oncology (Solid Tumors) PRAME (A02) Phase 1/2 ongoing (Ovarian, NSCLC)

The strategy for these Question Marks is clear: invest heavily to rapidly gain market share, which in this context means successfully navigating clinical trials to achieve regulatory approval. For instance, the Type 1 Diabetes candidate, IMC-S118AI, is targeted for a Clinical Trial Application (CTA) submission by the end of 2025.

The expansion of Brenetafusp into non-melanoma solid tumors, such as ovarian cancer and NSCLC, via Phase 1/2 trials represents an unproven expansion of a known molecule, fitting the high-risk, low-share profile of a Question Mark. The company is actively enrolling patients in these combination trials.

The financial reality is that these programs are currently losing money, as evidenced by the net loss of ($0.2) million for Q3 2025, despite strong product sales. The $70.6 million R&D spend in the quarter is the direct investment required to try and convert these Question Marks into future Stars.


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