Cellectar Biosciences Q3 net loss widens on higher R&D costs
Overview
US cancer drug developer's Q3 net loss widened year-over-year
Higher R&D expenses driven by Phase 3 trial preparations and ongoing CLR 125 activity
Company says cash balance sufficient to fund operations into Q2 2027
Outlook
Company on track to dose first patients in Phase 3 iopofosine I 131 trial in Q1 2027
Cellectar plans to file for accelerated FDA approval for iopofosine I 131 in 1H 2027
Company expects cash balance to fund operations into Q2 2027
Result Drivers
PHASE 3 TRIAL PREPARATIONS - Increased R&D expenses driven by initiation of Phase 3 confirmatory trial of iopofosine I 131 in Waldenström macroglobulinemia and ongoing Phase 1b CLR 125 trial in TNBC
CLINICAL DATA UPDATES - Presented updated efficacy and safety data for iopofosine I 131 in relapsed/refractory Waldenström macroglobulinemia, highlighting high response rates and durable outcomes
PIPELINE ADVANCEMENT - Initiated new clinical trials and advanced preparations for broader PDC platform programs
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Loss Per Share | $0.46 | ||
Q3 Net Loss | $8 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 4 "strong buy" or "buy", no "hold" and no "sell" or "strong sell"
The average consensus recommendation for the pharmaceuticals peer group is "buy"
Wall Street's median 12-month price target for Cellectar Biosciences Inc is $10.50, about 720.3% above its November 9 closing price of $1.28
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(This story was created using Reuters automation and AI based on LSEG and company data. It was checked and edited by a Reuters journalist prior to publication.)