Welcome to our dedicated page for Cellectar Biosciences news (Ticker: CLRB), a resource for investors and traders seeking the latest updates and insights on Cellectar Biosciences stock.
Cellectar Biosciences Inc (CLRB) operates at the intersection of oncology and nuclear medicine, developing radiopharmaceutical therapies for cancer treatment. The company's news flow reflects the characteristic milestones of clinical-stage biotechnology firms: financing announcements, clinical trial progress updates, regulatory interactions, and strategic partnerships. For investors tracking CLRB, understanding these news categories helps contextualize the company's development trajectory.
Financing announcements constitute a recurring news theme for Cellectar, as clinical-stage companies rely on capital markets to fund operations. News about public offerings, private placements, and at-the-market equity programs directly impacts share count and cash runway. These financing events often correlate with upcoming clinical milestones or general operational needs, providing insight into the company's capital requirements and financial planning.
Clinical development updates represent value-driving news for biotechnology investors. Protocol submissions, patient enrollment progress, data readouts, and regulatory designation announcements signal advancement of therapeutic candidates through development stages. For Cellectar specifically, news about iopofosine I 131 trials in hematologic malignancies and CLR 125 development in solid tumors indicates the pace of clinical progress. FDA interactions, including orphan drug designations and rare pediatric disease designations, suggest regulatory pathways and potential commercial advantages.
Partnership and supply agreement announcements reveal Cellectar's operational strategy, particularly regarding radioisotope procurement. Alpha-emitting isotopes face supply constraints industry-wide, making supply agreements for actinium-225 and astatine-211 material to the company's ability to advance alpha-PDC candidates. These partnerships also indicate the company's prioritization among pipeline candidates and therapeutic modalities.
Regulatory filings and corporate governance news, including SEC Form 4 insider transaction reports, proxy statements, and material event disclosures, provide transparency into company operations and management activities. For a clinical-stage biopharmaceutical trading on NASDAQ, these regulatory disclosures offer insight into corporate decision-making and shareholder matters beyond clinical development.
Cellectar Biosciences (NASDAQ: CLRB) announced a $1.98 million grant from the National Cancer Institute to expand its Phase 1 study of iopofosine I-131 in pediatric patients with inoperable high-grade gliomas. The funding supports the transition to Part 1b of the study, focusing on optimal dosing after initial efficacy signals from Part 1a. HGGs are aggressive brain tumors with poor prognoses. Iopofosine delivers radioisotopes directly to cancer cells, showing promising early results, including extended progression-free survival for patients.
Cellectar Biosciences (NASDAQ: CLRB) announced promising findings from the Phase 2 CLOVER-1 study of iopofosine I-131 in patients with quad-class refractory multiple myeloma who failed anti-BCMA therapies. The study revealed an overall response rate (ORR) of 50% among seven patients with a median of nine prior therapies. The mean overall survival was reported at 9.1 months. Safety assessments indicated manageable side effects with no treatment discontinuations. The company aims to leverage these results to expand iopofosine's application in treating aggressive hematologic cancers.
Cellectar Biosciences, Inc. (NASDAQ: CLRB) reported its financial results for Q2 2022, highlighting a significant milestone in the Phase 2B trial of iopofosine for Waldenstrom's macroglobulinemia. The independent data monitoring committee recommended continuation of the trial. As of June 30, 2022, the company had $24.8 million in cash, down from $35.7 million at the end of 2021. R&D expenses were $4.5 million for Q2 2022, consistent with the previous year, while G&A expenses rose to $2.9 million, reflecting higher costs. The net loss for the quarter was $7.4 million, compared to $6.0 million in Q2 2021.
Cellectar Biosciences (Nasdaq: CLRB) announced a reverse stock split effective July 22, 2022, consolidating every ten shares into one new share. Post-split, approximately 6.1 million shares will be outstanding while the ticker symbol and par value remain unchanged. Stockholder rights will stay the same except for fractional shares, which will be cashed out. The company aims to enhance its share value and improve trading liquidity amid its ongoing development of targeted cancer therapies, particularly iopofosine, currently in pivotal clinical studies.
Cellectar Biosciences, Inc. (NASDAQ: CLRB) reported financial results for Q1 2022, emphasizing the continuation of its pivotal Phase 2b trial of iopofosine for Waldenstrom’s macroglobulinemia (WM) after a positive assessment from an independent data monitoring committee. The company had cash and equivalents of $30.6 million as of March 31, 2022. Net loss for the quarter was $6.1 million, down from $6.4 million in Q1 2021. R&D expenses decreased to approximately $3.9 million, while G&A expenses rose to $2.3 million, reflecting increased professional fees.
Cellectar Biosciences (NASDAQ: CLRB) announced that an independent Data Monitoring Committee has completed a futility/efficacy assessment of its pivotal Phase 2b study of iopofosine in Waldenstrom’s macroglobulinemia (WM) and recommended continuation. The study aims to enroll 50 patients, focusing on a primary endpoint of a 20% major response rate. Cellectar noted an encouraging 83.3% major response rate in a prior study. The pivotal trial will assess treatment-free survival and duration of response, further advancing Cellectar's mission in targeted cancer therapies.
Cellectar Biosciences has announced the appointments of Matthew Hagan as Vice President, Marketing and Strategic Alliances, and David Lasecki as Executive Director, Strategic Alliances. Both bring extensive experience in oncology therapeutics, which the company believes will aid its transition to a commercial-stage entity. Cellectar's pivotal trial for iopofosine, targeting Waldenstrom’s macroglobulinemia, is ongoing, with interim data expected soon. The company continues to develop its Phospholipid Drug Conjugate platform, aiming to enhance cancer treatment efficacy while reducing side effects.
Cellectar Biosciences, Inc. (NASDAQ: CLRB) reported its 2021 financial results, showing a net loss of $24.1 million, or $0.43 per share, up from a $15.1 million loss in 2020. The company highlighted data from its Phase 2 CLOVER-1 study of iopofosine I-131, revealing a 45.5% overall response rate in multiple myeloma patients. Notable progress was made in a Phase 1 study involving children with relapsed high-grade gliomas, with positive tumor response and a recommendation to proceed with higher dosing. Cellectar maintains a strong balance sheet with $35.7 million in cash to fund operations into 2023.
Cellectar Biosciences (NASDAQ: CLRB) announced its participation in upcoming investor conferences, including the Roth Capital Partners 34th Annual Conference on March 15, 2022, and the Oppenheimer 32nd Annual Healthcare Conference on March 16, 2022. Both events will feature fireside chats and opportunities for 1x1 meetings with investors. Cellectar is focused on developing innovative cancer treatments using its proprietary Phospholipid Drug Conjugate platform, with ongoing studies on its lead asset, iopofosine, targeting various cancer types, including Waldenstrom's macroglobulinemia and pediatric cancers.
Cellectar Biosciences (NASDAQ: CLRB) has appointed Chad Kolean as Chief Financial Officer and promoted Jarrod Longcor to Chief Operating Officer. Kolean returns after a successful tenure at other companies, aiming to leverage his extensive industry experience. Longcor, with six years at Cellectar, will oversee operations and strategic growth efforts as the company prepares for a potential NDA filing for its drug targeting Waldenstrom’s macroglobulinemia. The company also plans a pivotal trial assessment of its lead compound, iopofosine I-131, in the near future.
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