Company profile for Acrivon Therapeutics

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About

Acrivon Therapeutics is a precision oncology therapeutics company uniquely enabled by a differentiated proteomics-based patient selection platform. Our method is widely applicable across drug classes and modalities. We specifically apply our approach to challenging oncology drug targets causally implicated in the vast majority of cancers, particularly those without simple single gene driver mutations or synthetic lethal contex...
Acrivon Therapeutics is a precision oncology therapeutics company uniquely enabled by a differentiated proteomics-based patient selection platform. Our method is widely applicable across drug classes and modalities. We specifically apply our approach to challenging oncology drug targets causally implicated in the vast majority of cancers, particularly those without simple single gene driver mutations or synthetic lethal contexts. Leveraging our unique patient selection platform, Acrivon Therapeutics aims to rapidly progress in-licensed clinical-stage assets and a pipeline of internally developed programs

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CONTACT DETAILS

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U.S.A
Address
Address
Watertown, MA, USA 480 Arsenal Way Suite 100 Watertown, MA 02472
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Telephone
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NEWS #PharmaBuzz

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https://ir.acrivon.com/news-releases/news-release-details/acrivon-therapeutics-announce-clinical-update-its-ongoing-phase

PRESS RELEASE
17 Dec 2025

https://ir.acrivon.com/news-releases/news-release-details/acrivon-therapeutics-reports-third-quarter-2025-financial

PRESS RELEASE
13 Nov 2025

https://www.fiercebiotech.com/biotech/acrivon-stops-developing-lilly-castoff-ovarian-bladder-cancer-focus-endometrial

FIERCE BIOTECH
26 Mar 2025

https://ir.acrivon.com/news-releases/news-release-details/acrivon-therapeutics-reports-initial-positive-clinical-data-acr

PRESS RELEASE
24 Apr 2024

https://ir.acrivon.com/news-releases/news-release-details/acrivon-therapeutics-host-corporate-rd-event-highlighting-ap3

PRESS RELEASE
16 Apr 2024

https://ir.acrivon.com/news-releases/news-release-details/acrivon-therapeutics-presents-data-aacr-annual-meeting

PRESS RELEASE
10 Apr 2024

Drugs in Development

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Details:

ACR-368 (prexasertib), a potent, selective CHK1/2 inhibitor, is deprioritized for ovarian and bladder cancers as targets and will be redirected to testing in endometrial cancer.


Lead Product(s): Prexasertib,Gemcitabine

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase I/ Phase IIProduct Type: Miscellaneous

Sponsor: Undisclosed

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable March 26, 2025

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Details : ACR-368 (prexasertib), a potent, selective CHK1/2 inhibitor, is deprioritized for ovarian and bladder cancers as targets and will be redirected to testing in endometrial cancer.

Product Name : Undisclosed

Product Type : Miscellaneous

Upfront Cash : Inapplicable

March 26, 2025

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Details:

ACR-2316 is a drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of Neoplasms.


Lead Product(s): ACR-2316

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase IProduct Type: Undisclosed

Sponsor: Undisclosed

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable October 31, 2024

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Lead Product(s) : ACR-2316

Therapeutic Area : Oncology

Highest Development Status : Phase I

Partner/Sponsor/Collaborator : Undisclosed

Deal Size : Inapplicable

Deal Type : Inapplicable

Details : ACR-2316 is a drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of Neoplasms.

Product Name : Undisclosed

Product Type : Undisclosed

Upfront Cash : Inapplicable

October 31, 2024

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Details:

Gemcitabine is a Cytotoxic Drug drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Squamous Cell Carcinoma of Head and Neck.


Lead Product(s): Gemcitabine,ACR-368

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase IIProduct Type: Cytotoxic Drug

Recipient: Moffitt Cancer Center

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable September 19, 2024

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Details : Gemcitabine is a Cytotoxic Drug drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Squamous Cell Carcinoma of Head and Neck.

Product Name : Undisclosed

Product Type : Cytotoxic Drug

Upfront Cash : Inapplicable

September 19, 2024

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Details:

The proceeds will advance ACR-368 (prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in Phase 2 trials, and its preclinical pipeline, including ACR-2316.


Lead Product(s): Prexasertib,Gemcitabine

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase I/ Phase IIProduct Type: Miscellaneous

Sponsor: RA Capital Management

Deal Size: $130.0 million Upfront Cash: Undisclosed

Deal Type: Private Placement April 09, 2024

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BePharma
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Details : The proceeds will advance ACR-368 (prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in Phase 2 trials, and its preclinical pipeline, including ACR-2316.

Product Name : Undisclosed

Product Type : Miscellaneous

Upfront Cash : Undisclosed

April 09, 2024

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Details:

Acrivon is currently advancing its lead candidate, ACR-368 (prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2 trial across multiple tumor types.


Lead Product(s): Prexasertib,Gemcitabine

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase I/ Phase IIProduct Type: Miscellaneous

Sponsor: Jefferies

Deal Size: $99.4 million Upfront Cash: Undisclosed

Deal Type: Public Offering November 15, 2022

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Details : Acrivon is currently advancing its lead candidate, ACR-368 (prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2 trial across multiple tumor types.

Product Name : Undisclosed

Product Type : Miscellaneous

Upfront Cash : Undisclosed

November 15, 2022

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Details:

ACR-368 is a Cytotoxic Drug drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Ovarian Neoplasms.


Lead Product(s): ACR-368

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase IIProduct Type: Cytotoxic Drug

Sponsor: GOG Foundation

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable September 21, 2022

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Lead Product(s) : ACR-368

Therapeutic Area : Oncology

Highest Development Status : Phase II

Partner/Sponsor/Collaborator : GOG Foundation

Deal Size : Inapplicable

Deal Type : Inapplicable

Details : ACR-368 is a Cytotoxic Drug drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Ovarian Neoplasms.

Product Name : Undisclosed

Product Type : Cytotoxic Drug

Upfront Cash : Inapplicable

September 21, 2022

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Details:

Proceeds will support the clinical development of advanced Phase 2 lead asset ACR-368, a potent DNA Damage Response (DDR) inhibitor clinically validated in solid cancers, and in-house drug pipeline driven by the company’s proprietary platform technology.


Lead Product(s): Prexasertib,Gemcitabine

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase IIProduct Type: Miscellaneous

Sponsor: Wellington Management Company

Deal Size: $100.0 million Upfront Cash: Undisclosed

Deal Type: Series B Financing November 11, 2021

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Lead Product(s) : Prexasertib,Gemcitabine

Therapeutic Area : Oncology

Highest Development Status : Phase II

Partner/Sponsor/Collaborator : Wellington Management Company

Deal Size : $100.0 million

Deal Type : Series B Financing

Details : Proceeds will support the clinical development of advanced Phase 2 lead asset ACR-368, a potent DNA Damage Response (DDR) inhibitor clinically validated in solid cancers, and in-house drug pipeline driven by the company’s proprietary platform technolog...

Product Name : Undisclosed

Product Type : Miscellaneous

Upfront Cash : Undisclosed

November 11, 2021

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Details:

Acrivon intends to develop prexasertib (also called ACR-368) in accelerated clinical trials treating patients whose tumors are driven by, and depend on, dysregulated CHK1 and CHK2 using the OncoSignature® test.


Lead Product(s): Prexasertib,Gemcitabine

Therapeutic Area: Oncology Brand Name: Undisclosed

Study Phase: Phase IIProduct Type: Miscellaneous

Sponsor: Undisclosed

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable June 29, 2021

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BePharma
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BePharma
Not Confirmed

Details : Acrivon intends to develop prexasertib (also called ACR-368) in accelerated clinical trials treating patients whose tumors are driven by, and depend on, dysregulated CHK1 and CHK2 using the OncoSignature® test.

Product Name : Undisclosed

Product Type : Miscellaneous

Upfront Cash : Inapplicable

June 29, 2021

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