Immunocore Provides Business Update and Reports Full Year 2020 Financial Results
Immunocore (Nasdaq: IMCR) provided a business update reporting its full year 2020 financial results. The company received FDA Breakthrough Therapy Designation for tebentafusp in metastatic uveal melanoma, showing a significant overall survival improvement in a Phase 3 trial (HR=0.51). As of December 31, 2020, Immunocore had $177 million in cash and raised an additional $287 million from its IPO. Revenue grew to £30.1 million, while R&D expenses decreased to £74.8 million. The company expects to submit a Biologics License Application for tebentafusp in Q3 2021.
- Tebentafusp achieved FDA Breakthrough Therapy Designation.
- Phase 3 trial data shows superior overall survival (HR=0.51).
- Cash position of $177 million and an additional $287 million raised from IPO.
- Revenue increased to £30.1 million.
- Loss for 2020 was £74.1 million, though improved from £103.9 million in 2019.
- Ongoing R&D expenses remain high at £74.8 million.
Immunocore Provides Business Update and Reports Full Year 2020 Financial Results
Breakthrough Therapy Designation granted by the FDA for tebentafusp in unresectable or metastatic uveal melanoma
Tebentafusp Phase 3 randomized trial data subject of an oral presentation at
the American Association for Cancer Research (AACR) 2021 Annual Meeting
Cash position of
(OXFORDSHIRE, England & CONSHOHOCKEN, Penn. & ROCKVILLE, Md., US, 25 March 2021) Immunocore (Nasdaq: IMCR), a late-stage biotechnology company pioneering the development of a novel class of T cell receptor (TCR) bispecific immunotherapies designed to treat a broad range of diseases, including cancer, infectious and autoimmune disease, today announced its results for the full year ended December 31, 2020.
2020 Highlights (including post-period)
- Lead product candidate tebentafusp demonstrated superior overall survival (OS) in a Phase 3 randomized clinical trial in metastatic uveal melanoma (mUM) where the OS Hazard Ratio (HR) in the intent-to-treat population favored tebentafusp, HR=0.51 (
95% CI: 0.36, 0.71). Tebentafusp was granted Breakthrough Therapy Designation by the U.S. Food and Drug Administration (FDA) for unresectable or metastatic uveal melanoma, and the Company anticipates completion of the submission of a Biologics License Application (BLA) in the third quarter of 2021.
- Continued development of ImmTAC (Immune mobilizing monoclonal T-cell receptors Against Cancer) clinical portfolio for multiple tumor types; IMC-C103C is currently in the dose escalation phase of a Phase 1 clinical trial in MAGE-A4 expressing solid tumors, with initial data expected to be presented in the second half of 2021; IMC-F106C is currently in a Phase 1 study in patients with PRAME-expressing solid tumors, with initial data expected to be presented mid-year 2022.
- Dosing in a Phase 1 clinical trial for patients with chronic hepatitis B virus (HBV) is anticipated for mid-year 2021.
- Cash position of
$177 million as of December 31, 2020 with an additional$287 million in net proceeds raised from the Company’s initial public offering and a concurrent private placement in February 2021.
Bahija Jallal, Chief Executive Officer of Immunocore, said: “Reflecting on 2020, we have made great strides in the clinical advancement of TCR therapeutics. We believe the tebentafusp clinical data represent the first positive Phase 3 clinical trial for a TCR therapeutic and the first bispecific immune-oncology therapy with demonstrated overall survival advantage in any solid tumor. These results were a culmination of disciplined work by the Immunocore team and strong support by our investors. Our initial public offering in February enables us to accelerate the development of our pipeline of TCR therapeutics and the planned BLA submission of our lead candidate tebentafusp in patients with uveal melanoma, as well as begin early commercialization activities assuming regulatory approval.”
Key Pipeline Updates
Tebentafusp
In November 2020, the Company announced tebentafusp achieved the primary endpoint of superior overall survival compared to investigator’s choice in a randomized Phase 3 clinical trial (IMCgp100-202) in previously untreated metastatic uveal melanoma, a cancer that has historically proven to be insensitive to chemotherapy and other immunotherapies. The 378-patient study was unblinded by an independent data monitoring committee at the first pre-planned interim analysis when the OS Hazard Ratio (HR) in the intent-to-treat population favored tebentafusp, HR=0.51 (
In February 2021, tebentafusp was granted Breakthrough Therapy Designation by the FDA for unresectable or metastatic uveal melanoma. Additionally, in February 2021, the European Commission, upon recommendation of the EMA’s Committee for Orphan Medicinal Products (COMP) awarded tebentafusp Orphan Drug Designation for the treatment of uveal melanoma. Medicines that meet the EMA’s Orphan Drug Designation criteria qualify for several incentives, including ten years of market exclusivity, protocol assistance, and potentially reduced fees for regulatory activities.
In March 2021, the Company announced that Phase 3 data from IMCgp100-202 Phase 3 clinical trial would be the subject of an oral presentation in the Phase 3 clinical trials plenary session at the AACR Annual Meeting 2021 which will be held virtually on April 10, 2021.
Additional Clinical Programs
IMC-C103C - MAGE-A4
As of year-end 2020, 21 patients had been dosed in the dose escalation portion of the IMC-C103C Phase 1/2 clinical trial in patients with solid tumors. Early pharmacodynamics data indicate that IMC-C103C monotherapy is demonstrating biological activity at the doses currently under evaluation. The Company plans to present Phase 1 data from this trial in the second half of 2021.
The Company believes that IMC-C103C is the only clinical stage off-the-shelf therapy candidate in development against MAGE-A4—an X-chromosome-linked cancer/testis protein that is broadly expressed across a range of cancer indications, including non-small-cell lung cancer, among others. IMC-C103C is part of a co-development/co-promotion collaboration with Genentech under which Immunocore shares program costs and profits equally.
IMC-F106C – PRAME
As of year-end 2020, nine patients had been dosed in the dose escalation portion of the IMC-F106C Phase 1/2 clinical trial. The trial is designed to study the safety and preliminary activity of IMC-F106C as a monotherapy in patients with PRAME-expressing solid tumors. The Company plans to report initial Phase 1 data from this trial in mid-2022.
IMC-F106C is an ImmTAC targeting a PRAME derived peptide presented by HLA-A*02:01 and is the first off-the-shelf therapeutic targeting PRAME. PRAME has the highest expression frequency of all cancer/testis antigens across a range of solid and hematologic cancers, notably non-small-cell lung cancer, and its expression is generally identified as a poor prognostic feature. Immunocore retains full rights to IMC-F106C.
IMC-I109V – HBV
In August 2020, the Company announced the publication of novel therapeutic approach with the potential to provide a functional cure for chronic hepatitis B, in leading peer-reviewed journal, Hepatology. These data support on-target efficacy of the lead HBV ImmTAV against HBV-infected hepatocytes. The Company plans to initiate dosing in the single ascending dosing portion of the trial in mid-2021.
IMC-M113V – HIV
In 2020, the Company advanced IMC-M113V through GMP manufacturing and IND supporting pre-clinical studies for human immunosuppression virus (HIV). The Company’s HIV programs are funded by the Bill & Melinda Gates Foundation, and regulatory submission to enable clinical testing is anticipated in the second half of 2021.
GSK-01– NY-ESO
The GSK-01 NY-ESO Phase 1 dose escalation study to determine safety, and which is enrolling several different tumor types, is still ongoing. An expansion phase was planned to initiate once the Phase 1 dose escalation was complete. However, following a portfolio review, Immunocore, in collaboration with GSK, have jointly elected not to plan for or initiate the efficacy determining expansion phase of the trial. The expansion arm was planned to be conducted in synovial sarcoma, an ultra-rare disease which is already addressed by other assets in the Company’s portfolio including MAGE-A4 and PRAME. Consequently, GSK has forgone their option to acquire an exclusive license to the NY-ESO program and Immunocore will retain ownership of the asset. Immunocore plans to present the data from the Phase 1 study in 2022.
Corporate Updates
Fundraising and initial public offering on Nasdaq
In February 2021, the Company raised
In December 2020, the Company completed a
In November 2020, the Company closed a
In March 2020, the Company completed a
Financial Results
Cash and cash equivalents at December 31, 2020 totaled
Revenue for the year ended December 31, 2020 from collaboration agreements was
For the year ended December 31, 2020, our research and development expenses were
The Company anticipates that its existing cash and cash equivalents, together with the net proceeds from its initial public offering and its debt facility, is sufficient to enable the Company to fund planned operating expenses and capital expenditure requirements through at the least the end of 2022.
##
About Immunocore
Immunocore is a late-stage biotechnology company pioneering the development of a novel class of TCR bispecific immunotherapies called ImmTAX – Immune mobilizing monoclonal TCRs Against X disease – designed to treat a broad range of diseases, including cancer, infectious and autoimmune. Leveraging its proprietary, flexible, off-the-shelf ImmTAX platform, Immunocore is developing a deep pipeline in multiple therapeutic areas, including five clinical stage programs in oncology and infectious disease, advanced pre-clinical programs in autoimmune disease and multiple earlier pre-clinical programs. Immunocore’s most advanced oncology therapeutic candidate, tebentafusp, has demonstrated an overall survival benefit in a randomized Phase 3 clinical trial in metastatic uveal melanoma, a cancer that has historically proven to be insensitive to other immunotherapies.
Forward Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including, but are not limited to, statements regarding the efficacy, safety and therapeutic potential of tebentafusp, the design, progress, timing, scope and results of the Company’s trials including IMCgp100-202, the anticipated timing of disclosure of results of clinical trials, plans for initiating future clinical trials and extension studies, the Company’s development programs including the discovery and development of new product candidates, the potential benefit of Breakthrough Therapy Designation or Orphan Drug Designation for tebentafusp, the timing of regulatory filings including estimates regarding the planned submission a BLA for tebentafusp, the likelihood of obtaining regulatory approval of any of the Company’s product candidates including tebentafusp, and the regulatory approval path for tebentafusp. Any forward-looking statements are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements, many of which are beyond the Company’s control. These risks and uncertainties include, but are not limited to, the impacts of the COVID-19 pandemic on the Company’s business, clinical trials and financial position; unexpected safety or efficacy data observed during preclinical studies or clinical trials; clinical trial site activation or enrollment rates that are lower than expected; changes in expected or existing competition; changes in the regulatory environment; and the uncertainties and timing of the regulatory approval process. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section titled “Risk Factors” in the Company’s final prospectus dated February 4, 2021 filed with the Securities and Exchange Commission pursuant to Rule 424(b)(4) on February 8, 2021, as well as discussions of potential risks, uncertainties, and other important factors in the Company’s subsequent filings with the Securities and Exchange Commission. All information in this press release is as of the date of the release, and the Company undertakes no duty to update this information, except as required by law.
CONTACT:
Immunocore
Debra Nielsen, Head of Communications
T: +1 (610) 368-8602
E: debra.nielsen@immunocore.com
Follow on Twitter: @Immunocore
Consilium Strategic Communications (corporate and financial)
Mary-Jane Elliott/ Chris Welsh/ Sukaina Virji
T: +44 (0)203 709 5700
E: Immunocore@consilium-comms.com
Investor Relations
Clayton Robertson, Head of Investor Relations
T: +1 215-384-4781
E: ir@immunocore.com
Immunocore Limited Annual report and consolidated financial statements
December 31, 2020
Consolidated Statements of Financial Position as at December 31,
| 2020 £’000 | 2019 £’000 | |||||||||
| Non-current assets | ||||||||||
| Property, plant and equipment | 13,754 | 18,302 | ||||||||
| Right of use assets | 23,093 | 36,578 | ||||||||
| Investment in sub-lease | 776 | 591 | ||||||||
| Other non-current financial assets | 4,410 | 4,390 | ||||||||
| Deferred tax asset | 2,230 | 1,507 | ||||||||
| Total non-current assets | 44,263 | 61,368 | ||||||||
| Current assets | ||||||||||
| Trade and other receivables | 10,280 | 9,639 | ||||||||
| Tax receivable | 12,935 | 40,410 | ||||||||
| Embedded derivative assets | - | 266 | ||||||||
| Cash and cash equivalents | 129,716 | 73,966 | ||||||||
| Total current assets | 152,931 | 124,281 | ||||||||
| Total assets | 197,194 | 185,649 | ||||||||
| Equity | ||||||||||
| Share capital | 1 | - | ||||||||
| Share premium | 386,230 | 283,250 | ||||||||
| Foreign currency translation reserve | 163 | (32 | ) | |||||||
| Share-based payment reserve | 18,821 | 10,659 | ||||||||
| Accumulated deficit | (349,869 | ) | (279,106 | ) | ||||||
| Total equity | 55,346 | 14,771 | ||||||||
| Non-current liabilities | ||||||||||
| Interest-bearing loans and borrowings | 36,654 | - | ||||||||
| Deferred liabilities | 24,868 | 47,961 | ||||||||
| Lease liabilities | 25,190 | 38,299 | ||||||||
| Provisions | 138 | 105 | ||||||||
| Total non-current liabilities | 86,850 | 86,365 | ||||||||
| Current liabilities | ||||||||||
| Interest-bearing loans and borrowings | - | 19,157 | ||||||||
| Trade and other payables | 25,728 | 29,501 | ||||||||
| Deferred liabilities | 27,118 | 28,522 | ||||||||
| Tax payable | - | 72 | ||||||||
| Lease liabilities | 2,043 | 1,951 | ||||||||
| Derivative liabilities | - | 5,127 | ||||||||
| Provisions | 109 | 183 | ||||||||
| Total current liabilities | 54,998 | 84,513 | ||||||||
| Total liabilities | 141,848 | 170,878 | ||||||||
| Total equity and liabilities | 197,194 | 185,649 | ||||||||
Immunocore Limited
Annual report and consolidated financial statements
December 31, 2020
Consolidated Statements of Loss and Other Comprehensive Income
for the years ended December 31,
| 2020 | 2019 | 2018 | ||||||||||||||||||||||||
| £ | ’000 | £ | ’000 | £ | ’000 | |||||||||||||||||||||
| Revenue | 30,114 | 25,669 | 23,654 | |||||||||||||||||||||||
| Total revenue | 30,114 | 25,669 | 23,654 | |||||||||||||||||||||||
| Net other operating income | 4,242 | 185 | 622 | |||||||||||||||||||||||
| Research and development costs | (74,809 | ) | (99,991 | ) | (83,575 | ) | ||||||||||||||||||||
| Administrative expenses | (45,740 | ) | (44,183 | ) | (34,156 | ) | ||||||||||||||||||||
| Operating loss | (86,193 | ) | (118,320 | ) | (93,455 | ) | ||||||||||||||||||||
| Other income | — | — | 4,979 | |||||||||||||||||||||||
| Finance income | 2,208 | 1,510 | 1,140 | |||||||||||||||||||||||
| Finance costs | (3,375 | ) | (9,379 | ) | (842 | ) | ||||||||||||||||||||
| Non-operating (expense) / income | (1,167 | ) | (7,869 | ) | 5,277 | |||||||||||||||||||||
| Loss before taxation | (87,360 | ) | (126,189 | ) | (88,178 | ) | ||||||||||||||||||||
| Income tax credit | 13,267 | 22,258 | 16,548 | |||||||||||||||||||||||
| Loss for the year | (74,093 | ) | (103,931 | ) | (71,630 | ) | ||||||||||||||||||||
| Other comprehensive (expense) / income | ||||||||||||||||||||||||||
| Exchange differences on translation of foreign operations | 195 | (99 | ) | 72 | ||||||||||||||||||||||
| Income tax effect relating to the components of other comprehensive income | — | — | 3,634 | |||||||||||||||||||||||
| Total other comprehensive (expense) / income for the year, net of tax | 195 | (99 | ) | 3,706 | ||||||||||||||||||||||
| Total comprehensive loss for the year, net of tax | (73,898 | ) | (104,030 | ) | (67,924 | ) | ||||||||||||||||||||
| Basic and diluted loss per share - £ | (2.79 | ) | (4.66 | ) | (3.32 | ) | ||||||||||||||||||||
Cash Flows
The following table summarizes the primary sources and uses of cash for each period presented:
| Year ended December 31, | ||||||||||||||||
| | 2020 | 2019 | 2018 | |||||||||||||
| $ | 000 | £ | 000 | £ | 000 | £ | 000 | |||||||||
| Cash and cash equivalents at beginning of the year | 101,052 | 73,966 | 124,385 | 82,883 | ||||||||||||
| Net cash used in operating activities | (82,756 | ) | (60,574 | ) | (101,376 | ) | (16,626 | ) | ||||||||
| Net cash provided by / (used in) investing activities | 638 | 467 | (4,137 | ) | 58,014 | |||||||||||
| Net cash provided by financing activities | 158,399 | 115,941 | 55,127 | 101 | ||||||||||||
| Foreign exchange on cash held | (115 | ) | (84 | ) | (33 | ) | 13 | |||||||||
| Cash and cash equivalents at end of the year | 177,218 | 129,716 | 73,966 | 124,385 | ||||||||||||
FAQ
What is Immunocore's cash position as of December 31, 2020?
What are the key results from the Phase 3 trial of tebentafusp?
When does Immunocore plan to submit its Biologics License Application for tebentafusp?
What was the revenue for Immunocore in 2020?
How much funding did Immunocore raise from its IPO?
