CLR 121125 (CLR 125): Auger Emitter (125I)
A next-generation investigational phospholipid ether (PLE) conjugate designed for highly localized radiation delivery through Auger electron emission.
Program Overview
CLR 125 is an investigational radioconjugate designed to deliver iodine-125 directly into tumor cell nucleus using Cellectar’s proprietary phospholipid ether (PLE) platform.
Iodine-125 emits Auger electrons—high-energy, short-range particles capable of inducing clustered/larger DNA double-strand breaks within targeted tumor cells while essentially eliminating any dose to surrounding healthy tissue.
Key Points
- Utilizes Cellectar’s PLE platform for selective tumor targeting
- Delivers Auger electrons (<1 µm range) for precision intracellular damage
- Designed to limit off-target exposure
- Structurally similar to iopofosine I-131, supporting development continuity
Mechanism of Action
How Auger Emitters Work
Auger emitters release multiple low-energy electrons that travel a few nanometers within cells, creating dense, localized energy deposits that disrupt tumor DNA.
CLR 125’s selective uptake enables potent, targeted damage with limited off target effects.
Scientific Highlights
- Short penetrating power requires intracellular delivery for efficacy
- Causes double-strand DNA breaks, similar to alpha emitters
- Generates additional reactive-oxygen–mediated activity
- Short emission distance may reduce off-target effects
| Name | Composition | Primary Mechanism of Cell Death | Penetrating Power (Emission Distance) | Relative Biologic Effect |
|---|---|---|---|---|
| Alpha Particles |
2 protons |
Double strand |
50 – 100um |
~5 |
| Beta Particles |
1 electron |
Single strand |
12mm |
1 |
| Auger Electrons |
Multiple electrons |
Double strand |
2 – 500nm |
1 – 5 |
Properties of different emitters provide enhanced outcomes
Preclinical Findings
Validated Intracellular Delivery with CLR 121125
In preclinical studies, CLR 125 showed selective tumor uptake and statistically significant activity in animal models of triple-negative breast cancer (TNBC), with no observed end-organ or hematologic toxicity at evaluated doses.
Highlights
- Selective tumor localization confirmed by imaging
- Dose-dependent growth inhibition or volume reduction at 1.2 mCi and 2.0 mCi
- No signs of end-organ or hematologic toxicity
Validated intracellular delivery with CLR 121125
Clinical Evaluation
Phase 1b Dose-Finding Study in Relapsed Triple-Negative Breast Cancer
CLR 125 is currently being studied in a Phase 1b imaging and therapy trial for patients with relapsed or refractory triple-negative breast cancer (TNBC). The study, a multi-center study including the Mayo Clinic Network, aims to determine the recommended Phase 2 dose and evaluate safety and tolerability.
Study Overview
- Study Overview
- Population: TNBC patients with progressive disease and no standard treatment options
- Primary Endpoint: Recommended Phase 2 dose
- Secondary Endpoints: Safety, tolerability, RECIST v1.1 and PFS, biodistribution
Key Eligibility Criteria
- Confirmed TNBC
- ≥ 1 measurable lesion > 10 mm
- ≥ 2 weeks since prior therapy
- No ongoing Grade ≥ 2 adverse events
Development Pathway
Expanding Cellectar’s Radiotherapeutic Platform
CLR 125 represents the continued evolution of Cellectar’s PLE platform, extending its precision-targeting approach across multiple isotope classes—beta (I-131), alpha (Ac-225), and Auger (I-125).
