Radiance Biopharma


Privately held biotechnology company focused on design and clinical development of next-generation antibody–drug conjugates (ADCs) and related biologics for oncology. The company develops bispecific and monospecific ADC formats, nanobody-based ADCs, monoclonal antibodies against tumor-specific biomarkers, companion diagnostics, and pursues IND submissions and Phase I clinical development in multiple territories.

Industries

N/A

Nr. of Employees

small (1-50)

Radiance Biopharma

One Boston Place, Ste. 2600, Boston, MA 02108, USA


Products

RB-601 (c-MET / EGFR bispecific nanobody ADC)

Bispecific nanobody-based ADC targeting c-MET and EGFR using site-specific conjugation to deliver a homogeneous DAR and an MMAE payload; cleared for IND in China and subject to first-in-human studies.

RB-164 (ROR-1 targeted ADC)

Fc-silenced ADC targeting ROR-1 with site-specific conjugation and a novel linker to deliver homogeneous DAR and enhanced stability; progressed into Phase I dose-escalation trials with IND clearances reported.

RB-201 (HER2 / TROP-2 bispecific ADC)

Bispecific ADC targeting HER2 and TROP-2 for tumors co-expressing these antigens; demonstrated superior efficacy versus monospecific ADCs in preclinical models and planned first-in-human Phase Ia/b clinical trial.

RB-203 (membrane Hsp70 monoclonal antibody and companion diagnostic)

Monoclonal antibody recognizing membrane Hsp70 that selectively accumulates in tumors expressing this biomarker; paired with a patented blood ELISA test to detect exosomal Hsp70 for tumor detection and response monitoring.

Expertise Areas

  • Antibody–drug conjugate development
  • Bispecific antibody engineering
  • Nanobody therapeutics
  • Monoclonal antibody therapeutics
  • Show More (6)

Key Technologies

  • Antibody–drug conjugates (ADCs)
  • Bispecific antibody formats
  • Nanobody-based therapeutics
  • Site-specific conjugation
  • Show More (6)

News & Updates

Press release reporting an exclusive license agreement for a first-in-class c-MET/EGFR targeted nanobody ADC.

News article reporting a proposed transaction for rights to a next-generation ADC.

Press release announcing first patient dosing in a Phase I dose-escalation trial of an ROR-1 targeted ADC.

Press release reporting FDA clearance of an IND application for an ROR-1 targeted ADC to support Phase I clinical development.

Press release describing an exclusive licensing transaction for a ROR-1 targeted ADC.

Announcement of a collaboration agreement with a contract research / biologics services provider for bispecific ADC development.


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