Cellectar Biosciences and ITM Enter Supply Agreement for GMP-Grade Actinium-225
CLRB(NASDAQ:CLRB) Supports Clinical Development of CLR 121225, Actinium-Labeled Compound for the Treatment of Solid Tumors
Supports Clinical Development of CLR 121225, Actinium-Labeled Compound for the Treatment of Solid Tumors
Cellectar Biosciences to Present Data in Poster Presentation at the American Association for Cancer Research Special Conference on Advances in Pancreatic Cancer Research
CLRB(NASDAQ:CLRB) FLORHAM PARK, N.J., Sept. 03, 2025 (GLOBE NEWSWIRE) -- Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage clinical biopharmaceutical company focused on the discovery and development of drugs for the treatment of cancer, today announced the acceptance of an abstract for poster presentation at the American Association for Cancer Research (AACR) Special Conference on Pancreatic Cancer Research taking place September 28-October 1 in Boston, Massachusetts. The poster presentation will highlight preclinical data from CLR 121225, the Company’s novel actinium-based radio conjugate alpha-emitter for treatment in hypoxic pancreatic ductal adenocarcinoma.
Cellectar Biosciences to Present Data in Oral Session and Panel Discussions at the American Association for Cancer Research Special Conference on Discovery and Innovation in Pediatric Cancer
CLRBPresenting Data from CLOVER-2 Phase 1 Clinical Study Evaluating Iopofosine I 131 in Relapsed/Refractory Pediatric High-Grade Glioma (r/r pHGG) Patients
Presenting Data from CLOVER-2 Phase 1 Clinical Study Evaluating Iopofosine I 131 in Relapsed/Refractory Pediatric High-Grade Glioma (r/r pHGG) Patients
Cellectar Biosciences Reports Second Quarter 2025 Financial Results and Provides a Corporate Update
CLRBIntend to Pursue an NDA Submission to the U.S. FDA under Accelerated Approval Pathway for Iopofosine I 131 for the Treatment of Waldenstrom Macroglobulinemia (WM) Subject to Sufficient Funding and Once the Confirmatory Trial is Underway
Cellectar Biosciences to Report Second Quarter Financial Results and Host a Conference Call on Thursday, August 14, 2025
CLRBFLORHAM PARK, N.J., Aug. 07, 2025 (GLOBE NEWSWIRE) -- Cellectar Biosciences, Inc. (NASDAQ: CLRB), a late-stage clinical biopharmaceutical company focused on the discovery, development and commercialization of drugs for the treatment of cancer, today announced that the Company will report financial results for the second quarter ended June 30, 2025, and provide a corporate update on August 14, 2025, at 8:30 a.m. Eastern Time.
Cellectar Biosciences Announces One-for-Thirty Reverse Stock Split
CLRBFLORHAM PARK, N.J., June 18, 2025 (GLOBE NEWSWIRE) -- Cellectar Biosciences, Inc. (Nasdaq: CLRB), a late-stage clinical biopharmaceutical company focused on the discovery and development of drugs for the treatment of cancer, today announced a one-for-thirty reverse stock split (the “Reverse Stock Split”) of the company’s common stock, par value $0.00001, which will become effective at 12:01 a.m. Eastern Time on Tuesday, June 24, 2025. The company’s common stock will continue to trade under its current trading symbol, CLRB, on the Nasdaq Global Select Market (“Nasdaq”) on a split-adjusted basis when the market opens on Tuesday, June 24, 2025, with the new CUSIP number 15117F880.
Cellectar Biosciences Reports Initial Phase 1 Results For Iopofosine I-131 In Relapsed Pediatric High-Grade Glioma, Showing Extended Survival And Disease Control In CLOVER-2 Trial
CLRBCellectar Biosciences Enters Into Definitive Agreements To Raise $2.5M From Sale Of Shares Priced At-Market For Nasdaq Purposes
CLRBWhat's Behind Cellectar Biosciences' Stock Surge? FDA Update Explained
CLRBCellectar's Iopofosine I 131 earned FDA breakthrough therapy designation for relapsed Waldenstrom macroglobulinemia following strong trial data.
US Stocks Higher; Dollar Tree Shares Plunge After Q1 Earnings
CLRBCellectar's Iopofosine I-131 Granted FDA Breakthrough Therapy Designation For Relapsed/Refractory Waldenstrom Macroglobulinemia Based On CLOVER WaM Phase 2 Study Showing 83.6% Response Rate; EMA Guidance On Conditional Approval Pathway Expected By Late Ju
CLRBMaxim Group Downgrades Cellectar Biosciences to Hold
CLRBCellectar Biosciences Q1 EPS $(0.14) Beats $(0.16) Estimate, Cash $13.9M
CLRBInsights Ahead: Cellectar Biosciences's Quarterly Earnings
CLRBCellectar Biosciences To Explore Strategic Alternatives
CLRBCellectar Biosciences Says Its Cash Balance Of $23.3M As Of December 31, 2024, Is Adequate To Fund Its Basic Budgeted Operations Into The Fourth Quarter Of 2025
CLRBCellectar Biosciences FY 2024 GAAP EPS $(1.40) Beats $(1.59) Estimate
CLRBReported Earlier, Cellectar Highlights Path Toward Accelerated Approval For Iopofosine I 131 and Expands Radioconjugate Development
CLRBOppenheimer Maintains Outperform on Cellectar Biosciences, Lowers Price Target to $12
CLRBCellectar Biosciences' Q3 Cash And Cash Equivalents Of $34.3M Is Expected To Provide Cash Runway Into Q2 2025
CLRBCellectar Biosciences Q3 2024 GAAP EPS $(0.40) Misses $(0.37) Estimate
CLRBCellectar Biosciences Signs Supply Agreement With NorthStar Medical Radioisotopes; NorthStar To Provide Co. With Non-Carrier Added Ac-225 For Its Clinical Programs
CLRBCellectar Biosciences Received A Letter From Nasdaq Informing The Company That It Had Regained Compliance With Nasdaq Listing Rule 5250(c)(1)
CLRBCellectar Biosciences Granted U.S. Patent #11,439,709 Phospholipid Ether Analogs as Cancer-targeting Drug Vehicles
CLRBCellectar Announces Publication Of Data from Its Expansion Cohort of the Phase II CLOVER-1 Study Iopofosine I-131 In Relapsed/Refractory Multiple Myeloma In Nature's Blood Cancer Journal
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