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Intellectia

BOLD News

Boundless Bio Q4 Earnings Miss Expectations

Mar 09 2026seekingalpha

Analysis of Growth Drivers in the Biliary Tract Cancer Market

Mar 02 2026Newsfilter

Boundless Bio Reports Second Quarter 2025 Financial Results and Business Highlights

Aug 05 2025Newsfilter

Rice Biotech Launch Pad welcomes Carolyn Ng to external advisory board

Jul 31 2025Newsfilter

Boundless Bio to Participate in the Goldman Sachs 46th Annual Global Healthcare Conference

Jun 05 2025Newsfilter

Leerink Partners Downgrades Boundless Bio to Market Perform, Lowers Price Target to $3

May 28 2025Benzinga

Boundless Bio Announces Portfolio Prioritization and Runway Extension

May 23 2025Newsfilter

Guggenheim Sticks to Its Hold Rating for Boundless Bio Inc. (BOLD)

Mar 30 2025Business Insider

BOLD Events

03/09 07:10
Boundless Bio Initiates BBI-940 Clinical Trial
"With the KOMODO-1 trial of BBI-940 actively enrolling, we are excited to evaluate this potentially first-in-class oral Kinesin degrader in patients with breast cancer who are seeking new treatment options. BBI-940 is designed to disrupt ecDNA segregation and inheritance, a differentiated mechanism for targeting chromosomally unstable cancers. The Boundless team is focused on clinical execution and reaching an initial proof-of-concept readout within our existing cash runway," said Zachary Hornby, President and Chief Executive Officer of Boundless Bio.
03/09 07:10
Company Cash and Short-term Investments Total $107.6 Million
Cash, cash equivalents, and short-term investments totaled $107.6 million as of December 31, 2025. The Company expects its cash to fund operations into the second half of 2028, through the anticipated initial clinical proof-of-concept readout from KOMODO-1.
01/20 07:20
Boundless Bio Halts Enrollment in BBI-355 and BBI-825 Trial
Following a strategic portfolio review, Boundless Bio has elected to cease enrollment of the Phase 1/2 Potentiate trial evaluating the combination of BBI-355, its oral, selective CHK1 inhibitor and BBI-825, its oral, selective RNR inhibitor, in oncogene-amplified cancers. "This decision reflects market considerations, clinical data, and the Company's prioritization of programs with the greatest potential to deliver meaningful clinical impact and long-term value," the company said.
01/20 07:20
Boundless Bio's BBI-940 IND Accepted by FDA, Clinical Trial to Start in 2026
Boundless Bio announced that the U.S. Food and Drug Administration, FDA, has accepted its Investigational New Drug, IND, application for its novel Kinesin oral degrader program, BBI-940. The acceptance of the BBI-940 IND enables Boundless to advance the program into a first-in-human clinical trial for patients with metastatic breast cancer, KOMODO-1, which is expected to initiate in the first half of 2026. The Company expects to deliver initial proof-of-concept clinical data within its cash runway timeline. Based on the revised operating plan, the Company's streamlined operations will extend its operating runway into the second half of 2028, through the anticipated initial clinical proof of concept readout for BBI-940.

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