Acimtamig with AlloNK® shows 86% response rate in relapsed/refractory classical Hodgkin lymphoma, with manageable safety.
Quiver AI Summary
Affimed N.V. announced promising results from a study combining acimtamig with Artiva Biotherapeutics’ allogeneic NK cell therapy, AlloNK®, for patients with relapsed/refractory classical Hodgkin lymphoma (R/R cHL). In the LuminICE-203 clinical trial, 22 heavily pretreated patients exhibited an overall response rate of 86%, with a complete response rate of 55%. The treatment demonstrated a manageable safety profile, with no unexpected safety signals or cases of graft-versus-host disease. This study is ongoing, and Affimed's Chief Medical Officer emphasized the significant potential of this combination as a new therapeutic option for patients who have exhausted prior standard treatments. These findings align with prior positive results from a related trial, underscoring the efficacy of acimtamig and AlloNK® in a multicenter setting.
Potential Positives
- The combination of acimtamig with AlloNK® demonstrated a high overall response rate of 86% and a complete response rate of 55% in heavily pretreated patients with relapsed/refractory classical Hodgkin lymphoma (R/R cHL).
- The treatment regimen exhibited a well-manageable safety profile with no unexpected safety signals, and importantly, no cases of graft-versus-host disease (GvHD) or immune effector cell-associated neurotoxicity syndrome (ICANS) were reported.
- This data reinforces the potential of acimtamig combined with AlloNK® as a viable treatment option for patients who have failed all standard treatment protocols.
- The findings were derived from a multicenter trial, enhancing the credibility and generalizability of the results across different patient populations and clinical settings.
Potential Negatives
- The reliance on a small sample size of only 22 heavily pretreated patients raises concerns about the generalizability of the results to the broader patient population.
- Despite reporting high response rates, the press release notes that all patients were heavily pretreated, suggesting limited treatment options remain for these individuals and possibly indicating the lack of efficacy in earlier treatment lines.
- The forward-looking statements section contains numerous uncertainties, including potential challenges related to ongoing clinical trials and regulatory approvals, which could affect the company's future prospects.
FAQ
What is the overall response rate of acimtamig with AlloNK® in the study?
The combination showed an overall response rate of 86% in the study of heavily pretreated patients.
How many patients were involved in the acimtamig and AlloNK® study?
The study included 22 heavily pretreated patients with relapsed/refractory classical Hodgkin lymphoma.
What is the complete response rate reported in the study?
The complete response rate for the combination treatment was reported at 55%.
Were there any unexpected safety signals reported in the trial?
No unexpected safety signals were observed, indicating a well-managed safety profile for the treatment.
What is the primary focus of Affimed N.V. as a company?
Affimed N.V. focuses on developing therapies that enhance the innate immune system to fight cancer effectively.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
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Full Release
- The combination of acimtamig with AlloNK ® demonstrated an overall response rate of 86% and complete response of 55% in 22 heavily pretreated patients with R/R cHL, who have exhausted all standard of care treatments
- The combination showed a well-manageable safety profile with no unexpected safety signals
MANNHEIM, Germany, Dec. 08, 2024 (GLOBE NEWSWIRE) -- Affimed N.V. (Nasdaq: AFMD) (“Affimed”, or the “Company”), a clinical-stage immuno-oncology company committed to giving patients back their innate ability to fight cancer, today announced the presentation of data in a poster session at the 66th ASH Annual Meeting and Exposition. The dataset includes 22 patients from the run-in phase of the LuminICE-203 (AFM13-203) phase 2 open-label, multicenter, multi-cohort study. The trial evaluates the safety and efficacy of the combination of acimtamig (AFM13) with Artiva Biotherapeutics’ allogeneic NK cell AlloNK ® in patients with R/R cHL.
Acimtamig in combination with AlloNK ® demonstrated a high overall response rate (ORR) of 86% with complete response (CR) of 55%. All patients in the study were heavily pretreated with a median of 5 (range: 2-13) prior therapies. All patients had received intensive combination chemotherapy, PD(L)1 checkpoint inhibitors and brentuximab vedotin. In addition, about two third of the patients had also received a previous stem cell transplant. The combination regimen exhibited a well-managed safety profile with no unexpected safety signals. Importantly, no cases of graft-versus-host disease (GvHD) or immune effector cell-associated neurotoxicity syndrome (ICANS) were reported.
“We are excited to present this new data, which highlights the significant potential of acimtamig combined with AlloNK ® as a highly effective, innovative treatment option for patients with R/R cHL,” said Dr. Andreas Harstrick, Chief Medical Officer of Affimed. “There are no established treatment options for patients with R/R cHL who have failed combination chemotherapy, PD(L)1 and brentuximab vedotin. To see more than 50% of patients achieving a complete response is extremely encouraging and highlights the potential that this combination may provide an effective treatment option for these refractory patients. It is also important that these data were obtained in a multicenter trial with 10 sites across the U.S. enrolling patients.”
These findings are in line with previous data generated from the single center investigator-initiated study AFM13-104 (NCT04074746), which utilized fresh allogeneic NK cells precomplexed with acimtamig in a similar R/R cHL patient population. These results further validate the co-administration approach of acimtamig with an off-the-shelf, allogeneic, cryopreserved NK cell product (AlloNK ® ) in a multi-center setting. Enrolment into the LuminICE-203 trial is ongoing.
About Acimtamig
Acimtamig (AFM13) is a first-in-class ICE ® that uniquely activates the innate immune system to destroy CD30-positive hematologic tumors. Acimtamig induces specific and selective killing of CD30-positive tumor cells, leveraging the power of the innate immune system by engaging and activating natural killer (NK) cells and macrophages. Acimtamig is a tetravalent bispecific innate cell engager designed to act as a bridge between the innate immune cells and the tumor, creating the necessary proximity for the innate immune cells to destroy the tumor cells.
About LuminICE-203 (AFM13-203)
LuminICE-203 (AFM13-203) is a Phase 2 open-label, multicenter, multi-cohort study. The trial is evaluating the safety and efficacy of the combination of acimtamig (AFM13) with Artiva Biotherapeutics’ allogeneic NK cell AlloNK ® (AB-101) in patients with relapsed/refractory classical Hodgkin lymphoma and CD30-positive peripheral T cell lymphoma (NCT05883449).
The study builds on the unprecedented efficacy results from an investigator sponsored study, AFM13-104, which investigated acimtamig in combination with cord blood-derived NK cells in patients with refractory/recurrent CD30-positive Hodgkin or non-Hodgkin lymphoma (NCT04074746).
About Affimed N.V.
Affimed (Nasdaq: AFMD) is a clinical-stage immuno-oncology company committed to giving patients back their innate ability to fight cancer by actualizing the untapped potential of the innate immune system. The Company’s innate cell engagers (ICE ® ) enable a tumor-targeted approach to recognize and kill a range of hematologic and solid tumors. ICE ® are generated on the Company’s proprietary ROCK ® platform which predictably generates customized molecules that leverage the power of innate immune cells to destroy tumor cells. A number of ICE ® molecules are in clinical development, being studied as mono- or combination therapy. Headquartered in Mannheim, Germany, Affimed is led by an experienced team of biotechnology and pharmaceutical leaders united by the bold vision to stop cancer from ever derailing patients’ lives. For more about the Company’s people, pipeline and partners, please visit: www.affimed.com .
Forward-Looking Statements
This press release contains forward-looking statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as “anticipate,” “believe,” “could,” “estimate,” “expect,” “goal,” “intend,” “look forward to,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “will,” “would” and similar expressions. Forward-looking statements appear in a number of places throughout this release and include statements regarding the Company’s intentions, beliefs, projections, outlook, analyses and current expectations concerning, among other things, the potential of acimtamig (AFM13), AFM24, AFM28 and the Company’s other product candidates; the value of its ROCK ® platform; its ongoing and planned clinical trials; its corporate restructuring, the associated headcount reduction and the impact this may have on Company’s anticipated savings and total costs and expenses; its collaborations and development of its products in combination with other therapies; the timing of and its ability to make regulatory filings and obtain and maintain regulatory approvals for its product candidates; its intellectual property position; its collaboration activities; its ability to develop commercial functions; clinical trial data; its results of operations, cash needs, financial condition, liquidity, prospects, future transactions, growth and strategies; the industry in which it operates; the macroeconomic trends that may affect the industry or the Company, such as the instability in the banking sector experienced in the first quarter of 2023; impacts of the COVID-19 pandemic, the benefits to Affimed of orphan drug designation; the impact on its business by political events, war, terrorism, business interruptions and other geopolitical events and uncertainties, such as the Russia-Ukraine conflict; the fact that the current clinical data of acimtamig in combination with NK cell therapy is based on acimtamig precomplexed with fresh allogeneic cord blood-derived NK cells from The University of Texas MD Anderson Cancer Center, as opposed to Artiva’s AB-101; and other uncertainties and factors described under the heading “Risk Factors” in Affimed’s filings with the SEC. Given these risks, uncertainties, and other factors, you should not place undue reliance on these forward-looking statements, and the Company assumes no obligation to update these forward-looking statements, even if new information becomes available in the future.
Affimed Investor Relations Contact
Alexander Fudukidis
Director, Investor Relations
E-Mail: a.fudukidis@affimed.com
Tel.: +1 (917) 436-8102
Affimed Media Contact
Mary Beth Sandin
Vice President, Marketing and Communications
E-Mail: m.sandin@affimed.com