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Intellectia

ACRV News

Acrivon Therapeutics Q4 Earnings Miss Expectations

Mar 19 2026seekingalpha

Acrivon Therapeutics Reports Promising Preclinical Results

Mar 17 2026Yahoo Finance

FDA's Accelerated Approval Framework Drives Cancer Treatment Advances

Feb 17 2026Newsfilter

Oncolytics Biotech Strengthens Leadership Amid Oncology Market Surge

Jan 28 2026PRnewswire

Oncolytics Biotech Strengthens Leadership to Advance Clinical Programs

Jan 28 2026Newsfilter

ScinoPharm Secures FDA Approval for Glatiramer Acetate Injection in Multiple Sclerosis

Jan 09 2026NASDAQ.COM

Acrivon Therapeutics (ACRV) Shares Plunge 28.71% Following Mixed Phase 2b Clinical Results

Jan 08 2026NASDAQ.COM

Acrivon Updates ACR-368 Phase 2 Data, Reports 39% ORR in Endometrial Cancer

Jan 08 2026Benzinga

ACRV Events

03/19 07:30
Company Cash and Investments Reach $118.6 Million, Sufficient to Fund Until Q2 2027
As of December 31, 2025, the company had cash, cash equivalents and investments of $118.6 million, which is expected to fund operating expenses and capital expenditure requirements into the second quarter of 2027.
03/19 07:30
Company Plans to Initiate Fourth Cohort of ACR-368 Study in H1 2026
Building on clinical data and observed biomarker upregulation in serous EC, the company announced today that it plans to initiate a fourth cohort in the ongoing ACR-368 Phase 2b study in the first half of 2026. This arm will enroll all-comer serous EC subjects, similar to Arm 3, but subjects will be treated with ACR-368 monotherapy and otherwise identical inclusion criteria to Arm 3. Company also announced today that it has completed the exploratory Arm 2 of the study which treated BM- EC subjects with less than or equal to3 prior LoT using ACR-368 with ULDG sensitization. Objectives of this arm were achieved, supporting that ULDG may contribute to ACR-368 efficacy in BM- subjects with a favorable tolerability profile.
03/19 07:30
Acrivon CEO Highlights ACR-368's Potential in Endometrial Cancer
"It's an exciting time for the company as we build on strong maturing data and clinical momentum," said Peter Blume-Jensen, M.D., Ph.D., chief executive officer, president, and founder of Acrivon. "Our compelling data from ACR-368 in EC was well received at the ESGO Congress, reinforced by powerful commentary from world-renowned key opinion leaders at our live webcast, after the late-breaking oral presentation by Dr. Konstantinopoulos from the Dana- Farber Cancer Institute. Serous EC represents a particularly significant unmet need with a mortality rate resulting in 40-50% of all EC deaths. Through our rapidly maturing data, we are strategically generating multiple opportunities towards potential registration for ACR-368, including our announcement today of a fourth arm to our study to investigate ACR-368 monotherapy in biomarker-unselected serous EC subjects. Elsewhere in our pipeline, ACR-2316 has already shown promising clinical activity in lung cancer, underscoring the potential of its differentiated mechanism of action. Finally, we continue to build our pipeline with our next development candidate, ACR-6840, and new programs, reflecting our sustained AP3-driven innovation and commitment to long-term value creation."

ACRV Monitor News

Acrivon Therapeutics Surges on Upcoming Clinical Data Presentation

Jan 08 2026

ACRV Earnings Analysis

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