Ready 8-Ks
23
Latest filing
May 13, 2026, 4:10 PM ET
Top materiality
0.85
Event mix
other_material ×12 · earnings ×8 · leadership ×2
Sentiment
12 pos · 0 neg · 11 neu
Latest earnings
reported 2026-Q1
-
Acrivon Q1 net loss $19.0M; cash $97.7M; key ACR-368 interim readout in H2 2026
Net loss $19.0M vs $19.7M YoY; R&D $15.2M, G&A $4.7M.
-
Acrivon Therapeutics Q4/FY2025 net loss $19M/$77.9M; cash $118.6M; ACR-368 52% cORR in serous EC
Net loss Q4 $19.0M, FY $77.9M; cash and securities $118.6M expected to fund into Q2 2027.
-
Acrivon terminates Akoya/Quanterix diagnostic deal; opens internal CLIA lab
Mutually terminated OncoSignature Companion Diagnostic Agreement with Akoya (Quanterix) effective Feb 25, 2026.
-
ACR-368 interim data from registrational-intent arms presented at ESGO for endometrial cancer serous subtype
Interim data from ACR-368 Phase 2b registrational-intent trial presented at ESGO Congress on February 27, 2026.
-
Acrivon reports positive ACR-368 Phase 2b data in serous EC; ACR-2316 shows tumor shrinkage in Phase 1
ACR-368 Phase 2b: 39% ORR overall; in serous EC ≤2 prior lines, cORR 52% (N=23) and 67% in BM+ (N=12). Arm 3 expanding to EU, enrollment complete Q4 2026.
-
Acrivon Therapeutics Provides Clinical Data Updates for ACR-368 and Initial ACR-2316 Data
On January 8, 2026, Acrivon hosted a webcast and conference call featuring ACR-368 clinical data and program updates.
-
Acrivon Therapeutics Q3 2025 net loss $18.2M, cash $134.4M to fund into Q2 2027
Net loss of $18.2M for Q3 2025, improved from $22.4M in Q3 2024.
-
Acrivon reports new mouse-model data showing complete tumor regression and immune memory for ACR-368 and ACR-2316 combos
Syngeneic mouse model: sustained complete tumor regression and immune memory after multiple implant rounds over ~1 year.
-
Acrivon Q2 net loss $21.0M, cash $147.6M; advances ACR-368 and ACR-2316 trials
Net loss of $21.0M for Q2 2025, up from $18.8M in Q2 2024; R&D spend $16.2M.
-
Acrivon stockholders elect three Class III directors and ratify PwC as auditor
Quorum of 29,659,010 shares (94.59%) present at 2025 annual meeting on June 13.
-
Acrivon's ACR-368 shows 35% cORR in endometrial cancer; cash $164.8M
Q1 2025 net loss $19.7M vs $16.5M YoY; R&D spend $15.4M on trial advancement.
-
Acrivon Therapeutics appoints Mansoor Raza Mirza as CMO effective April 9, 2025
Dr. Mirza is a gynecologic oncology KOL who led registrational trials for Zejula (PARP inhibitor) and frontline endometrial cancer therapy.
-
Acrivon reports Q4/FY24 net loss $22.8M/$80.6M; ACR-368 endometrial cancer cORR 35% in BM+ patients
Cash $184.6M as of Dec 31, 2024; runway extended into 2027.
-
Acrivon reports ACR-368 35% ORR in refractory endometrial cancer; deprioritizes ovarian/bladder
Preliminary cash, cash equivalents and ST investments ~$184.6M as of Dec 31, 2024; runway into 2027.
-
Acrivon appoints Adam Levy as CFO; Rasmus Holm-Jorgensen steps down effective April 1, 2025
Rasmus Holm-Jorgensen resigns as CFO effective April 1, 2025, for personal reasons to pursue Europe-based opportunity; no disagreement.
-
Acrivon reports Q3 net loss $22.4M; ACR-368 shows 62.5% ORR in endometrial cancer
Net loss Q3 2024: $22.4M vs $14.5M in Q3 2023; R&D expenses rose to $18.9M from $10.3M.
-
Acrivon doses first patient in Phase 1 trial of WEE1/PKMYT1 inhibitor ACR-2316
First patient dosed two quarters ahead of original timeline for ACR-2316 Phase 1 trial in solid tumors.
-
ACR-368 endometrial cancer Phase 2: 62.5% ORR in OncoSignature+ patients; ACR-2316 IND cleared
Confirmed ORR of 62.5% (95% CI 30.4-86.5) in prospectively-selected OncoSignature+ endometrial cancer patients who progressed on anti-PD-1.
-
Acrivon Q2 net loss $18.8M; $220.4M cash; ACR-368 Phase 2 shows 50% ORR
Net loss of $18.8M vs $13.9M YoY; R&D expenses $15.0M, G&A $6.4M.
-
Acrivon Therapeutics stockholders elect three Class II directors and ratify PwC as auditor at 2024 annual meeting
Kristina Masson, Sharon Shacham, and Ivana Magovčević-Liebisch were elected as Class II directors with 24.6M, 23.3M, and 24.5M votes in favor, respectively.
-
Acrivon Q1 net loss $16.5M; ACR-368 Phase 2b 50% ORR; $130M PIPE
Net loss $16.5M vs $12.8M YoY; R&D $11.5M, G&A $6.2M.
-
Acrivon reports 50% confirmed ORR with ACR-368 in OncoSignature-positive gynecological cancers; cash ~$234M
Phase 2b: 50% confirmed ORR in OncoSignature-positive ovarian/endometrial (10 pts), 0% ORR in negative (16), p=0.0038.
-
Acrivon nets ~$130M in PIPE; shares at $8.50, pre-funded warrants for 7.1M shares
Gross proceeds ~$130M from 8.235M shares at $8.50/share and 7.06M pre-funded warrants at $8.499/warrant.