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Context Therapeutics Reports Second Quarter 2025 Operating and Financial Results

Key Takeaway: Context Therapeutics Inc. has reported its operating and financial results for the second quarter of 2025, showcasing ongoing Phase 1 studies for bispecific antibodies CTIM-76 and CT-95. The company confirmed it has sufficient cash reserves to fund operations into 2027 and expects to report initial dose escalation data from these trials in 2026. However, they also noted an increase in net losses and rising R&D expenses, primarily attributed to advancements in their development pipeline.

Market Sentiment Analysis

POSITIVE FACTORS

  • Context Therapeutics has a robust cash position of $83.5 million, ensuring funding into 2027.
  • Upcoming clinical data for CTIM-76 and CT-95 is anticipated, highlighting progress in the pipeline.
  • The company has expanded its operations, including the appointment of a new Chief Medical Officer.

CONCERNS & RISKS

  • The company reported a significant net loss of $8.8 million for Q2 2025, an increase from the previous year.
  • R&D expenses rose sharply, particularly due to costs related to new product candidates CT-95 and CT-202.

Full Press Release Details

CTIM-76 and CT-95 Phase 1 dose-escalation studies ongoing
Cash and cash equivalents of $83.5 million as of June 30, 2025
Company expects its cash and cash equivalents will continue to fund operations into 2027
PHILADELPHIA, Aug. 06, 2025 (GLOBE NEWSWIRE) -- Context Therapeutics Inc. (“Context” or the “Company”) (Nasdaq: CNTX), a clinical-stage biopharmaceutical company advancing T cell engaging bispecific antibodies for solid tumors, today announced its financial results for the second quarter ended June 30, 2025, and reported on recent and upcoming business highlights.
“We remain focused on progressing our clinical pipeline — CTIM-76, a selective Claudin 6 (“CLDN6”) x CD3 bispecific antibody, and CT-95, an avidity enhanced mesothelin (“MSLN”) x CD3 bispecific antibody,” said Martin Lehr, CEO of Context. “We expect to share initial dose escalation data for the CTIM-76 trial in the second quarter of 2026 and for the CT-95 trial by mid-2026.”
“We also expect to complete necessary regulatory filings to support the initiation of a first-in-human trial for CT-202, a potential best-in-class Nectin-4 x CD3 bispecific antibody, in the second quarter of 2026,” Mr. Lehr continued. “With cash runway into 2027, we believe we are well-positioned to achieve our goal of advancing our portfolio of innovative T cell-engaging therapies for solid tumors.”
Second Quarter 2025 Highlights
In June 2025, presented a Trial in Progress poster for the Phase 1 clinical trial evaluating CTIM-76 at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting.
In April 2025, presented preclinical and translational data for CT-95, a MSLN targeting T cell engager, at the American Association for Cancer Research (AACR) Annual Meeting 2025.
In April 2025, announced the first patient dosed in our Phase 1 clinical trial evaluating CT-95 in patients with MSLN-expressing advanced solid tumors, including ovarian, pancreatic, lung, and mesothelioma cancers.
Corporate Updates and Presentations
In June 2025, announced the appointment of Dr. Karen Chagin as Chief Medical Officer
In May 2025, presented at the Citizens Life Sciences Conference.
In April 2025, participated in the 24th Annual Needham Virtual Healthcare Conference.
Second Quarter 2025 Financial Results
Cash and cash equivalents were $83.5 million at June 30, 2025, compared to $94.4 million at December 31, 2024. The Company expects its cash and cash equivalents will be sufficient to fund its operations into 2027.
Research and development (“R&D”) expenses were $7.8 million for the second quarter of 2025, as compared to $1.4 million for the second quarter of 2024. The increase in R&D expenses was primarily driven by higher CT-202 expense of $3.1 million, higher CT-95 expense of $1.5 million and higher CTIM-76 expense of $0.1 million. CT-95 was acquired in July 2024 and CT-202 was in-licensed in September 2024. In addition, personnel-related costs increased by $1.6 million primarily due to higher headcount over the prior year period as well as termination benefits incurred related to employee departures.
General and administrative expenses were $1.9 million for the second quarter of 2025, as compared to $1.7 million for the second quarter of 2024. The increase was primarily driven by a $0.2 million increase in personnel-related costs, including share-based compensation, mainly due to higher headcount and compensation adjustments.
Other income was approximately $0.9 million for the second quarter of 2025, as compared to other income of $0.8 million for the second quarter of 2024, primarily due to higher interest income earned on cash and cash equivalent balances.
Context reported a net loss of $8.8 million for the second quarter of 2025, as compared to a loss of $2.3 million for the second quarter of 2024.
About Context Therapeutics®
Context Therapeutics Inc. (Nasdaq: CNTX) is a biopharmaceutical company advancing T cell engaging (“TCE”) bispecific antibodies for solid tumors. Context is building an innovative portfolio of TCE bispecific therapeutics, including CTIM-76, a Claudin 6 x CD3 TCE, CT-95, a Mesothelin x CD3 TCE, and CT-202, a Nectin-4 x CD3 TCE. Context is headquartered in Philadelphia. For more information, please visit www.contexttherapeutics.com or follow the Company on X (formerly Twitter) and LinkedIn.
Forward-looking Statements
This press release contains “forward-looking statements” that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, included in this press release regarding strategy, future operations, prospects, plans and objectives of management, including words such as “may,” “will,” “expect,” “anticipate,” “look forward,” “plan,” “intend,” and similar expressions (as well as other words or expressions referencing future events, conditions, or circumstances) are forward-looking statements. These include, without limitation, statements regarding (i) our expectation to share initial dose escalation data from the Phase 1 trials of CTIM-76 and CT-95 in the second quarter of 2026 and mid-2026, respectively, (ii) our expectation to complete necessary regulatory filings to support the initiation of a first-in-human trial for CT-202 in the second quarter of 2026, (iii) having sufficient cash and cash equivalents to fund our operations into 2027, (iv) the potential benefits, characteristics, and side effect profile of our product candidates, (v) the ability of our product candidates to have benefits, characteristics, and a side effect profile that is differentiated and/or better than third party product candidates, (vi) the likelihood data will support future development, and (vii) the likelihood of obtaining regulatory approval of our product candidates. Forward-looking statements in this release involve substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by the forward-looking statements, and we therefore cannot assure you that our plans, intentions, expectations, or strategies will be attained or achieved. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in our filings with the U.S. Securities and Exchange Commission, including the section titled “Risk Factors” contained therein. Except as otherwise required by law, we disclaim any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events, or circumstances or otherwise.
Context Therapeutics Inc.
Condensed Statements of Operations
(Unaudited)
Three Months Ended June 30, Six Months Ended June 30,
2025 2024 2025 2024
Operating Expenses
Research and development $ 7,830,544 $ 1,384,553 $ 11,293,535 $ 3,357,762
General and administrative 1,927,818 1,703,996 3,993,970 3,554,288
Loss from operations (9,758,362 ) (3,088,549 ) (15,287,505 ) (6,912,050 )
Other income 930,852 834,043 1,882,734 989,747
Net loss $ (8,827,510 ) $ (2,254,506 ) $ (13,404,771 ) $ (5,922,303 )
Net loss per common share, basic and diluted ($0.09 ) ($0.04 ) ($0.14 ) ($0.17 )
Weighted average shares outstanding, basic and diluted 95,186,935 54,958,635 95,186,935 35,462,344
Context Therapeutics Inc.
Condensed Balance Sheets Data
(Unaudited)
June 30, December 31,
2025 2024
Cash and cash equivalents $ 83,517,047 $ 94,429,824
Other assets 3,635,054 3,696,935
Total assets $ 87,152,101 $ 98,126,759
Total liabilities $ 4,607,779 $ 2,860,497
Total stockholders' equity 82,544,322 95,266,262
Total liabilities and stockholders' equity $ 87,152,101 $ 98,126,759
Investor Relations Contact:
Jennifer Minai-Azary
Context Therapeutics

Frequently Asked Questions

What clinical studies are currently ongoing at Context Therapeutics?

Context Therapeutics is currently conducting Phase 1 dose-escalation studies for CTIM-76 and CT-95.

How much cash does Context Therapeutics have as of June 2025?

As of June 30, 2025, Context Therapeutics reported cash and cash equivalents of $83.5 million.

When will initial data for CTIM-76 and CT-95 be shared?

Initial dose escalation data for CTIM-76 is expected in the second quarter of 2026 and for CT-95 by mid-2026.

Who was appointed Chief Medical Officer in June 2025?

Dr. Karen Chagin was appointed Chief Medical Officer of Context Therapeutics in June 2025.

What was the net loss for Context Therapeutics in Q2 2025?

Context Therapeutics reported a net loss of $8.8 million for the second quarter of 2025.

Last updated: Aug 6, 2025