CytomX Therapeutics Reports First Quarter 2024 Financial Results and Provides Business Update
CytomX Therapeutics reported positive initial Phase 1a dose escalation data for CX-904 in solid tumors, with ongoing dose escalation. Additionally, the first dose cohort for CX-2051 in solid tumors has been cleared, and the Phase 1 study continues. CX-801 is advancing to Phase 1 with a clinical collaboration agreement with Merck. The company achieved $10 million in milestones with Astellas. Financially, total revenue increased to $41.5 million, cash equivalents totaled $150.3 million, and research and development expenses increased slightly.
Positive initial Phase 1a dose escalation data for CX-904 in solid tumors with favorable safety profile and encouraging anti-cancer activity.
Cleared first dose cohort for CX-2051 in solid tumors with initial data expected in the first half of 2025.
Advancement of CX-801 to Phase 1 with a clinical collaboration agreement with Merck.
Achievement of $10 million in milestones with Astellas for preclinical progress.
Total revenue increased to $41.5 million, cash equivalents totaled $150.3 million by March 31, 2024.
Decrease in cash balance from $174.5 million to $150.3 million as of March 31, 2024.
Increase in research and development expenses by $0.9 million for the three months ended March 31, 2024.
- Company announces positive initial Phase 1a dose escalation data for monotherapy CX-904 (EGFRxCD3 T-cell engager) in solid tumors -
- First dose cohort cleared in Phase 1 clinical study of CX-2051, an EpCAM Targeting PROBODY® ADC, in solid tumors. Initial data anticipated in the first half of 2025 -
- Phase 1 study initiation activities continue for CX-801, an interferon alpha-2b PROBODY® cytokine, including the execution of a clinical collaboration agreement with Merck to supply KEYTRUDA® (pembrolizumab) for evaluation in combination with CX-801. Initial data anticipated in 2025 -
- Achieved
- Dr. Zhen Su appointed to Board of Directors -
- Management to hold conference call today at 5 p.m. EDT / 2 p.m. PDT -
SOUTH SAN FRANCISCO, Calif., May 08, 2024 (GLOBE NEWSWIRE) -- CytomX Therapeutics, Inc. (Nasdaq: CTMX), a leader in the field of masked, conditionally activated biologics, today reported first quarter 2024 financial results and provided a business update.
“CytomX’s multi-modality PROBODY® therapeutic pipeline encompasses some of the most exciting areas of current oncology R&D, including T-cell engagers, ADCs, and cytokines. CytomX’s leadership and continuous innovation in the field of masked, conditionally activated biologics ideally positions us to develop novel, potent therapies for cancer patients in key areas of unmet need,” said Sean McCarthy, D.Phil., chief executive officer and chairman of CytomX.
McCarthy added, “CytomX entered 2024 executing to our plan and with substantial momentum, looking towards key data readouts from our multi-modality PROBODY® therapeutic pipeline over the next 12 to 24 months. Our exciting announcement today of positive initial Phase 1a clinical data for CX-904 marks the beginning of this data-rich period and we look forward to making continued progress with our broad program of masked, PROBODY® T-cell engagers and to also demonstrating clinical proof of concept for CX-2051 and CX-801, for which we anticipate initial Phase 1 data in 2025.”
First Quarter Business Highlights and Recent Developments
Pipeline
CX-904, PROBODY® T-cell-engager (TCE) targeted to EGFRxCD3, demonstrates a favorable safety profile and encouraging anti-cancer activity in Phase 1 dose escalation. Dose escalation continues.
CX-904 is a conditionally activated PROBODY TCE designed to target the epidermal growth factor receptor (EGFR) on cancer cells and the CD3 receptor on T cells within the tumor microenvironment. CX-904 is being evaluated in an ongoing Phase 1 study.
Today, the Company announced positive initial Phase 1 dose escalation data in heavily pre-treated patients with advanced metastatic solid tumor types that are generally known to express EGFR. 19 patients were initially enrolled into non-step dosing cohorts with target doses ranging from 0.007 mg to 6 mg. 16 patients were subsequently enrolled into step-dosing cohorts with target doses ranging from 5 mg to 10 mg and with tocilizumab prophylaxis. Dose escalation continues and enrollment into a cohort with a target dose of 15 mg is ongoing.
- As of the April 16, 2024 data cutoff, CX-904 demonstrated a favorable safety profile including no observed cases of CRS of any grade in step-dosing cohorts and only Grade 1 CRS observed in patients treated at the highest non-step dose. The most common treatment-related adverse events (TRAEs) were arthralgia, arthritis, rash, pruritis, and vomiting, the majority of which were low grade.
- Eight patients had measurable tumor reduction, including 2 of 6 (
33% ) efficacy-evaluable pancreatic cancer patients with confirmed partial responses per RECIST 1.1. - Preliminary pharmacokinetic and pharmacodynamic data were consistent with the PROBODY TCE mechanism of action, including maintained masking in circulation, and CD8+ T-cell margination and tumor infiltration.
- CX-904 Phase 1a dose escalation and optimization continue, with future enrollment focused on determining a recommended Phase 2 dose.
- The Company expects to provide an additional Phase 1a dose escalation update by the end of 2024. These additional data will help inform next steps along with partner Amgen, towards initiation of Phase 1b expansion cohorts in specific EGFR positive tumor types.
CX-2051, an EpCAM-directed PROBODY® antibody drug conjugate, first patient dosed in Phase 1 in April 2024, initial data expected in 2025.
EpCAM is a promising oncology target with significant potential that is highly expressed across many indications including colorectal, gastric, endometrial, and ovarian cancers. EpCAM has been clinically validated by locally administered, previously approved cancer therapies. To date, systemically administered anti-EpCAM therapeutics have been unsuccessful due to toxicities in certain epithelial tissues. CX-2051 utilizes a cytotoxic payload that is a derivative of camptothecin, a topoisomerase-1 inhibitor, a class of drug that has shown potent clinical anti-cancer activity in the ADC context for multiple targets and cancer types. CX-2051 has demonstrated a wide predicted therapeutic index in multiple preclinical models, constituting an opportunity for broad clinical use in large patient populations.
- In April 2024, the first patient was dosed as part of the Phase 1 dose escalation of CX-2051 in patients with solid tumors generally known to express EpCAM, including CRC. The first dose cohort in the CX-2051 Phase 1 study has been cleared and dose escalation continues.
- The Phase 1 dose escalation study is following a Bayesian Optimal Interval (BOIN) design and is intended to demonstrate initial clinical proof of concept to inform a potential decision to move into dose expansion cohorts in 2025.
- Initial data for CX-2051 is expected in the first half of 2025.
CX-801, a dually-masked PROBODY® interferon-alpha 2b, advancing to Phase 1 in Q2 2024. Executed Clinical Collaboration Agreement with Merck (known as MSD outside of the US and Canada) to evaluate CX-801 in combination with Merck’s anti-PD-1 therapy KEYTRUDA® (pembrolizumab).
Interferon-alpha 2b is an immunotherapeutic cytokine that has demonstrated clinical activity and gained regulatory approval previously in multiple cancer types, including locally advanced or metastatic melanoma, renal cancer and bladder cancer. IFNα2b provides a potentially superior approach to activating anti-tumor immune responses compared to other cytokines but its clinical benefit has been limited to date by severe dose-limiting toxicities. CX-801 is an optimized, dually masked, conditionally activated IFNα2b, designed to have an expanded therapeutic index that has the potential to become a cornerstone of combination therapy for a wide range of tumor types.
- Announced a clinical collaboration agreement with Merck to supply KEYTRUDA for a Phase 1 study of CX-801 in combination with KEYTRUDA.
- CX-801 is anticipated to initiate Phase 1 dose escalation in patients with solid tumors including melanoma, renal, and head and neck squamous cell carcinoma in Q2 2024. The Phase 1 dose escalation will utilize a BOIN design to evaluate safety and signs of clinical activity for CX-801 monotherapy and for CX-801 in combination with KEYTRUDA.
- Initial Phase 1 data for CX-801 is expected in 2025.
KEYTRUDA® is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.
CytomX continues to make progress in its R&D partnerships.
CytomX has multiple active research and development partnerships and more than 10 ongoing research programs with major biotechnology and pharmaceutical companies (Amgen, Astellas, Bristol Myers Squibb, Moderna and Regeneron). The majority of these programs are focused on masked, conditionally activated PROBODY® T-cell engagers.
In Q1 2024, CytomX achieved
- A
$5.0 million milestone for the initiation of GLP toxicology studies for the first clinical candidate program in the collaboration. - A
$5.0 million milestone for the nomination of the second clinical candidate in the collaboration.
2024 Priorities and Key Milestones:
- CX-904 (EGFRxCD3):
- CX-904 Phase 1a dose escalation and optimization continue, with future enrollment focused on determining a recommended Phase 2 dose or doses.
- An additional Phase 1a dose escalation update is expected by the end of 2024.
- A potential decision, to be taken with Amgen, to initiate Phase 1b expansion cohorts in specific EGFR positive tumor types is expected by the end of 2024.
- CX-2051 (EpCAM):
- Continued Phase 1 dose escalation in solid tumors with known EpCAM expression.
- Initial Phase 1a data is expected in the first half 2025.
- CX-801 (IFNα2b):
- Initiation of Phase 1 dose escalation in solid tumors including melanoma, renal, and head and neck squamous cell carcinoma is expected by Q2 2024.
- Initial Phase 1a data is expected in 2025.
- Collaborations:
- Continuation of T-cell engager focused drug discovery and development activities with Bristol Myers Squibb, Amgen, Astellas, and Regeneron.
- Progress with Moderna on conditionally activated mRNA-based programs.
- Potential additional pre-clinical and clinical milestones in 2024 and beyond.
Q1 2024 Financial Results
Cash, cash equivalents and investments totaled
Total revenue was
Research and development expenses increased by
General and administrative expenses decreased by
Conference Call & Webcast
CytomX management will host a conference call and simultaneous webcast today at 5 p.m. EDT (2 p.m. PDT) to discuss the financial results and provide a business update. Participants may access the live webcast of the conference call from the Events and Presentations page of CytomX’s website at https://ir.cytomx.com/events-and-presentations. Participants may register for the conference call here and are advised to do so at least 10 minutes prior to joining the call. An archived replay of the webcast will be available on the company’s website.
About CytomX Therapeutics
CytomX is a clinical-stage, oncology-focused biopharmaceutical company focused on developing novel conditionally activated, masked biologics designed to be localized to the tumor microenvironment. By pioneering a novel pipeline of localized biologics, powered by its PROBODY® therapeutic platform, CytomX’s vision is to create safer, more effective therapies for the treatment of cancer. CytomX’s robust and differentiated pipeline comprises therapeutic candidates across multiple treatment modalities including antibody-drug conjugates (“ADCs”), T-cell engagers, and immune modulators such as cytokines. CytomX’s clinical-stage pipeline includes CX-904, CX-2051 and CX-801. CX-904 is a masked, conditionally activated T-cell-engaging bispecific antibody targeting the epidermal growth factor receptor (EGFR) on tumor cells and the CD3 receptor on T cells. CX-904 is partnered with Amgen in a global co-development alliance. CX-2051 is a masked, conditionally activated ADC directed toward epithelial cell adhesion molecule, EpCAM, with potential applicability across multiple EpCAM-expressing epithelial cancers. CX-2051 was discovered in collaboration with Immunogen, now part of AbbVie. CX-801 is a masked interferon alpha-2b PROBODY® cytokine with broad potential applicability in traditionally immuno-oncology sensitive as well as insensitive (cold) tumors. CytomX has established strategic collaborations with multiple leaders in oncology, including Amgen, Astellas, Bristol Myers Squibb, Regeneron and Moderna. For more information about CytomX and how it is working to make conditionally activated treatments the new standard-of-care in the fight against cancer, visit www.cytomx.com and follow us on LinkedIn and X (formerly Twitter).
CytomX Therapeutics Forward-Looking Statements
This press release includes forward-looking statements. Such forward-looking statements involve known and unknown risks, uncertainties and other important factors that are difficult to predict, may be beyond our control, and may cause the actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied in such statements, including those related to the future potential of partnerships or collaboration agreements. Accordingly, you should not rely on any of these forward-looking statements, including those relating to the potential benefits, safety and efficacy or progress of CytomX’s or any of its collaborative partners’ product candidates, including CX-904, CX-2051, and CX-801, the potential benefits or applications of CytomX’s PROBODY® therapeutic platform, CytomX’s or its collaborative partners’ ability to develop and advance product candidates into and successfully complete clinical trials, including the ongoing and planned clinical trials of CX-904, and the timing of the commencement of clinical trials or initial and ongoing data availability for CX-801 and CX-2051, and other development milestones. Risks and uncertainties that contribute to the uncertain nature of the forward-looking statements include: the unproven nature of CytomX’s novel PROBODY® therapeutic technology; CytomX’s clinical trial product candidates are in the initial stages of clinical development and its other product candidates are currently in preclinical development, and the process by which preclinical and clinical development could potentially lead to an approved product is long and subject to significant risks and uncertainties, including the possibility that the results of preclinical research and early clinical trials, including initial CX-904 results, may not be predictive of future results; the possibility that CytomX’s clinical trials will not be successful; the possibility that current preclinical research may not result in additional product candidates; CytomX’s dependence on the success of CX-904, CX-801, and CX-2051; CytomX’s reliance on third parties for the manufacture of the Company’s product candidates; possible regulatory developments in the United States and foreign countries; and the risk that we may incur higher costs than expected for research and development or unexpected costs and expenses. Additional applicable risks and uncertainties include those relating to our preclinical research and development, clinical development, and other risks identified under the heading "Risk Factors" included in CytomX’s Quarterly Report on Form 10-Q filed with the SEC on May 8, 2024. The forward-looking statements contained in this press release are based on information currently available to CytomX and speak only as of the date on which they are made. CytomX does not undertake and specifically disclaims any obligation to update any forward-looking statements, whether as a result of any new information, future events, changed circumstances or otherwise.
PROBODY is a U.S. registered trademark of CytomX Therapeutics, Inc.
Company Contact:
Chris Ogden
SVP, Finance and Accounting
cogden@cytomx.com
Investor Contact:
Stern Investor Relations
Stephanie Ascher
stephanie.ascher@sternir.com
Media Contact:
Redhouse Communications
Teri Dahlman
teri@redhousecomms.com
| CYTOMX THERAPEUTICS, INC. | |||||||
| CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | |||||||
| (in thousands, except share and per share data) | |||||||
| (Unaudited) | |||||||
| Three Months Ended | |||||||
| March 31, | |||||||
| 2024 | 2023 | ||||||
| Revenues | $ | 41,463 | $ | 23,499 | |||
| Operating expenses: | |||||||
| Research and development | 22,052 | 21,175 | |||||
| General and administrative | 7,754 | 7,977 | |||||
| Total operating expenses | 29,806 | 29,152 | |||||
| Income (Loss) from operations | 11,657 | (5,653 | ) | ||||
| Interest income | 2,194 | 2,327 | |||||
| Other (expense) income, net | (11 | ) | 15 | ||||
| Income (Loss) before income taxes | 13,840 | (3,311 | ) | ||||
| Provision for income taxes | 49 | — | |||||
| Net Income (loss) | 13,791 | (3,311 | ) | ||||
| Other comprehensive income (loss): | |||||||
| Unrealized (loss) gain on investments, net of tax | (105 | ) | 16 | ||||
| Total comprehensive income (loss) | $ | 13,686 | $ | (3,295 | ) | ||
| Net income (loss) per share: | |||||||
| Basic | $ | 0.17 | $ | (0.05 | ) | ||
| Diluted | $ | 0.17 | $ | (0.05 | ) | ||
| Shares used to compute net income (loss) per share | |||||||
| Basic | 82,029,466 | 66,248,992 | |||||
| Diluted | 82,630,020 | 66,248,992 | |||||
| CYTOMX THERAPEUTICS, INC. | |||||||
| CONDENSED BALANCE SHEETS | |||||||
| (in thousands) | |||||||
| March 31, | December 31, | ||||||
| 2024 | 2023 | ||||||
| (unaudited) | (1) | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 36,185 | $ | 17,171 | |||
| Short-term investments | 114,099 | 157,338 | |||||
| Accounts receivable | 13,177 | 3,432 | |||||
| Prepaid expenses and other current assets | 3,786 | 4,995 | |||||
| Total current assets | 167,247 | 182,936 | |||||
| Property and equipment, net | 3,567 | 3,958 | |||||
| Intangible assets, net | 693 | 729 | |||||
| Goodwill | 949 | 949 | |||||
| Restricted cash | 917 | 917 | |||||
| Operating lease right-of-use asset | 11,234 | 12,220 | |||||
| Other assets | 80 | 83 | |||||
| Total assets | $ | 184,687 | $ | 201,792 | |||
| Liabilities and Stockholders' Deficit | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 1,964 | $ | 1,458 | |||
| Accrued liabilities | 14,220 | 17,599 | |||||
| Operating lease liabilities - short term | 4,724 | 4,589 | |||||
| Deferred revenue, current portion | 123,628 | 132,267 | |||||
| Total current liabilities | 144,536 | 155,913 | |||||
| Deferred revenue, net of current portion | 59,743 | 80,048 | |||||
| Operating lease liabilities - long term | 8,148 | 9,385 | |||||
| Other long term liabilities | 3,940 | 3,893 | |||||
| Total liabilities | 216,367 | 249,239 | |||||
| Commitments and contingencies | |||||||
| Stockholders' deficit: | |||||||
| Convertible preferred stock | — | — | |||||
| Common stock | 1 | 1 | |||||
| Additional paid-in capital | 677,986 | 675,905 | |||||
| Accumulated other comprehensive (loss) income | (10 | ) | 95 | ||||
| Accumulated deficit | (709,657 | ) | (723,448 | ) | |||
| Total stockholders' deficit | (31,680 | ) | (47,447 | ) | |||
| Total liabilities and stockholders' deficit | $ | 184,687 | $ | 201,792 | |||
_____________
(1) The condensed balance sheet as of December 31, 2023 was derived from the audited financial statements included in the Company's Annual Report on Form 10-K for the year ended December 31, 2023.
FAQ
What positive results were reported for CX-904 in the press release?
What is the status of the CX-2051 Phase 1 study?
What milestone was achieved with Astellas mentioned in the press release?
How did the total revenue and cash equivalents change in the first quarter of 2024?
