Bristol Myers Squibb's Breyanzi Receives FDA Approval for Marginal Zone Lymphoma Treatment
Written by Emily J. Thompson, Senior Investment Analyst
Source: Newsfilter
Updated: 2 hour ago
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Source: Newsfilter
- Significant Efficacy: In the TRANSCEND FL study, Breyanzi demonstrated an overall response rate of 95.5% among 66 patients with relapsed or refractory marginal zone lymphoma, showcasing its exceptional effectiveness and solidifying its leading position in CD19-directed CAR T cell therapies.
- Good Safety Profile: The safety profile of Breyanzi was consistent with prior reports, with 76% of patients experiencing any grade of cytokine release syndrome (CRS), including 4.5% with grade 3 or higher, indicating its acceptability and manageable nature in clinical applications.
- Market Potential: Breyanzi is now the only CAR T cell therapy approved by the FDA for marginal zone lymphoma, marking its broad applicability in treating B-cell malignancies and is expected to drive further growth for the company in the cell therapy market.
- Patient Support: Bristol Myers Squibb offers various support programs to ensure broad coverage of Breyanzi and facilitate patients' treatment journeys, reflecting the company's deep commitment to understanding and addressing patient needs.
BMY.N$0.0000%Past 6 months

No Data
Analyst Views on BMY
Wall Street analysts forecast BMY stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for BMY is 52.67 USD with a low forecast of 36.00 USD and a high forecast of 68.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
Wall Street analysts forecast BMY stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for BMY is 52.67 USD with a low forecast of 36.00 USD and a high forecast of 68.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
Current: 50.960

Current: 50.960

William Blair
Matthew Phipps
Market Perform
maintain
Reason
William Blair
Matthew Phipps
William Blair analyst Matthew Phipps notes Bristol Myers today announced that its ADEPT-2 study evaluating Cobenfy in Alzheimer's disease psychosis will now read out by the end of 2026, versus prior timing for a readout by year-end 2025. The delay is due to the need for additional patient enrollment in the study given that irregularities were identified at several clinical trial sites, the analyst tells investors in a research note. Blair says that while a delay due to site irregularities typically raises concerns with investors, there is potentially a positive read-through in the Independent Data Monitoring Committee and Food and Drug Administration recommending continuation of the trial with more patients. This suggests positive trends are being observed, according to Blair. The firm thinks "any non-failure could be good news" given the selloff in Bristol Myers shares year-to-date. It has a Market Perform rating on the name. The stock in morning trading is up 5% to $50.76.
After Bristol Myers announced that it is delaying the readout of the ADEPT-2 study of Cobenfy in Alzheimer's Psychosis as it adds more patients to the trial due to irregularities at some clinical trial sites, JPMorgan said the firm is "not completely surprised by this update" and sees it as an incremental positive. Expectations were low on ADEPT-2, the additional patient-adds enhances the chances of a successful study and this does not impact the timing of the FDA filing based on the remaining ADEPT study readouts, according to the analyst, who maintain an Overweight rating on the shares.
Leerink analyst David Risinger notes that Bristol Myers announced that it will enroll additional patients in the ADEPT-2 study. The firm views it as positive news that the Data Monitoring Committee recommended enrolling additional patients in Cobenfy's ADEPT-2 trial in Alzheimer's disease psychosis patients. Recall that the company disclosed in early August that it was scrutinizing Cobenfy trial conduct, and Leerink and consensus feared the trial could fail. The firm keeps an Outperform rating on the shares.
Neutral
maintain
$51 -> $57
Reason
Goldman Sachs raised the firm's price target on Bristol Myers to $57 from $51 and keeps a Neutral rating on the shares.
About BMY
Bristol-Myers Squibb Company is a global biopharmaceutical company. It is engaged in the discovery, development and delivery of transformational medicines for patients facing serious diseases in areas: oncology, hematology, immunology, cardiovascular, neuroscience and other areas. Its growth portfolio includes Opdivo (nivolumab), Opdivo Qvantig (nivolumab and hyaluronidase-nvhy), Yervoy (ipilimumab), Reblozyl (luspatercept-aamt), Opdualag (nivolumab and relatlimab-rmbw), Breyanzi (lisocabtagene maraleucel), Camzyos (mavacamten), Zeposia (ozanimod), Abecma (idecabtagene vicleucel), and Sotyktu (deucravacitinib). Its other growth products include Onureg, Inrebic, and Empliciti. Its legacy portfolio includes Eliquis (apixaban), Revlimid (lenalidomide), Pomalyst/Imnovid (pomalidomide), Sprycel (dasatinib), and Abraxane (paclitaxel albumin-bound particles for injectable suspension). Opdivo (nivolumab) is a fully human monoclonal antibody that binds to the PD-1 on T and NKT cells.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.