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“The information we’re presenting at this yr’s ASCO mirror the breadth and depth of our oncology pipeline and our unwavering dedication to analysis that would remodel outcomes for sufferers going through most cancers,” mentioned Roopal Thakkar , M.D., government vice chairman, analysis and improvement and chief scientific officer, AbbVie. “These shows underscore our management in driving scientific innovation to handle a few of the most urgent unmet wants in oncology right this moment by leveraging our modern platforms similar to ADCs.”

An oral presentation on investigational telisotuzumab adizutecan (ABBV-400, Temab-A), a next-generation, c-Met directed antibody-drug conjugate (ADC) with a novel topoisomerase 1 inhibitor (Top1i) payload, will showcase:

• Preliminary security and efficacy ends in 41 sufferers with pre-treated, superior epidermal progress issue receptor (EGFR)-mutated non-squamous non-small cell lung most cancers (NSCLC) from the dose enlargement a part of a Section 1 research ( NCT05029882 ). ¹ Sufferers obtained a median of three prior traces of therapies and 93% of sufferers had prior anti-EGFR therapy. The target response price (ORR) was 63%. ¹ Excessive ORR was noticed no matter c-Met protein expression ranges. ¹ On the time of knowledge cut-off, 54% of responders skilled a ≥6 months length of response (DoR). ¹ The most typical any-grade TEAEs in ≥30% of sufferers had been anemia (63%), nausea (61%), vomiting (37%), decreased urge for food (34%), and neutropenia (34%). ¹ Extra knowledge with 4 months follow-up will probably be offered at ASCO.

  Temab-A can be being evaluated in a number of ongoing medical trials together with a Section 1/2 Research ( NCT06772623 ) in first-line NSCLC with out actionable genomic alterations together with budigalimab (AbbVie’s investigational programmed cell loss of life 1 inhibitor), a Section 2 research ( NCT06107413 ) in second-line metastatic colorectal most cancers (CRC) together with fluorouracil, folinic acid and bevacizumab, and a Section 3 research ( NCT06614192 ) as monotherapy in sufferers with c-Met overexpressing refractory metastatic CRC.

“The anti-tumor exercise of Temab-A in sufferers with pre-treated, superior EGFR-mutated non-squamous NSCLC is encouraging and helps additional exploration of this novel ADC on this setting,” mentioned Ross Camidge , M.D., Ph.D, College of Colorado Most cancers Middle, United States and principal investigator of the trial. “Temab-A seems to have a manageable security profile and continues to indicate promising medical exercise in superior NSCLC, which is related to poor prognosis.”

Extra oral shows will spotlight new security and efficacy knowledge for ABBV-706, a SEZ6-directed ADC with a Top1i payload, and pivekimab sunirine (PVEK), a novel ADC designed to focus on CD123:

• In a Section 1 open-label research of ABBV-706 monotherapy, 64 sufferers with high-grade neuroendocrine neoplasms (NENs), a various group of uncommon and aggressive stable tumors, obtained ABBV-706 monotherapy IV at 1.3–3.5 mg/kg as soon as each 3 weeks. ^2,3 Your complete cohort had an ORR of 31.3%, and a median DoR of 5.6 months. ² The most typical grade ≥3 TEAEs (cumulative throughout all dose ranges), had been anemia (45%), neutropenia (33%), and thrombocytopenia (21%). ² Extra knowledge will probably be offered at ASCO.

  This ongoing research ( NCT05599984 ) is evaluating ABBV-706 as monotherapy, or together with budigalimab, carboplatin, or cisplatin, in sufferers with superior stable tumors expressing SEZ6, together with small-cell lung most cancers, NENs and high-grade Central Nervous System tumors.

• Outcomes from the open-label, multicenter Section 1b /2 CADENZA trial ( NCT03386513 ) of PVEK monotherapy in sufferers with beforehand untreated or relapsed/refractory (R/R) blastic plasmacytoid dendritic cell neoplasm (BPDCN), a extremely aggressive and uncommon sort of blood most cancers, demonstrated medical profit. ^4,5 The outcomes present that amongst 33 untreated sufferers, the first endpoint of composite full response (CCR) price, outlined as CR + medical CR (CR with minimal pores and skin abnormality), was 70% (95% CI, 51.3-84.4) with a median length of CCR of 9.8 months. ORR was 85%. ⁴ Within the 51 sufferers with R/R BPDCN, the CCR price was 14% with a median length of CCR of 9.2 months. ORR was 35%. ⁴ Amongst all of the 84 sufferers enrolled, the most typical grade ≥3 TEAEs had been peripheral edema (12%). ⁴ TEAEs led to discontinuation in 9% and seven% of sufferers with first-line and R/R BPDCN, respectively. ⁴ Extra knowledge will probably be offered at ASCO.

  PVEK can be being evaluated in a Section 1/2 research ( NCT04086264 ) in R/R and newly identified acute myeloid leukemia.

“Over the previous few years, we have considerably expanded our ADC portfolio to analyze a broad vary of stable tumors and blood cancers, reflecting our deep dedication to reworking most cancers care by way of focused therapies and biomarker pushed approaches,” mentioned Daejin Abidoye, M.D., vice chairman, therapeutic space head of stable tumors, AbbVie. “These outcomes spotlight the potential of our investigational medicines to supply a significant medical profit in a number of difficult-to-treat cancers, the place present therapy choices are restricted.”

Additional data on AbbVie medical trials is out there at https://www.clinicaltrials.gov/ .

Extra particulars on key shows at ASCO can be found under and the total ASCO Annual Assembly 2025 abstracts can be found right here .

Telisotuzumab adizutecan, ABBV-706, pivekimab sunirine, etentamig, livmoniplimab, budigalimab, ABBV-291 and ABBV-969 are investigational medicines and are usually not permitted by any well being authorities worldwide. The security and efficacy of those investigational medicines are below analysis as a part of ongoing medical research.

Venetoclax, ibrutinib, epcoritamab, telisotuzumab vedotin are permitted medicines being investigated for extra makes use of. Security and efficacy haven’t been established for these unapproved further makes use of.

EPKINLY ^® /TEPKINLY ^® (epcoritamab) is being co-developed by Genmab and AbbVie as a part of the businesses’ oncology collaboration. The businesses share industrial duties within the U.S. and Japan, with AbbVie chargeable for additional world commercialization.

VENCLEXTA ^® /VENCLYXTO ^® (venetoclax) is being developed by AbbVie and Roche. It’s collectively commercialized by AbbVie and Genentech, a member of the Roche Group, within the U.S. and by AbbVie outdoors of the U.S.

IMBRUVICA ^® (ibrutinib) is collectively developed and commercialized by Pharmacyclics LLC, an AbbVie firm and Janssen Biotech, Inc.

U.S. Prescribing Info for AbbVie Medicines

Please see full Prescribing Info for EMRELIS ^™ (telisotuzumab vedotin-tllv)
Please see full Prescribing Info for EPKINLY ^® (epcoritamab-bysp)
Please see full Prescribing Info for IMBRUVICA ^® (ibrutinib)
Please see full Prescribing Info for VENCLEXTA ^® (venetoclax tablets)

About AbbVie
AbbVie’s mission is to find and ship modern medicines and options that remedy critical well being points right this moment and tackle the medical challenges of tomorrow. We try to have a exceptional influence on individuals’s lives throughout a number of key therapeutic areas together with immunology, oncology, neuroscience and eye care – and services and products in our Allergan Aesthetics portfolio. For extra details about AbbVie, please go to us at www.abbvie.com . Comply with @abbvie on LinkedIn,   Fb , Instagram , X (previously Twitter) and YouTube.

About AbbVie in Oncology
AbbVie is dedicated to elevating requirements of care and bringing transformative therapies to sufferers worldwide residing with difficult-to-treat cancers. We’re advancing a dynamic pipeline of investigational therapies throughout a variety of most cancers sorts in each blood cancers and stable tumors. We’re specializing in creating focused medicines that both impede the replica of most cancers cells or allow their elimination. We obtain this by way of varied, focused therapy modalities and biology interventions, together with small molecule therapeutics, antibody-drug conjugates (ADCs), immuno-oncology-based therapeutics, multispecific antibody and novel CAR-T platforms. Our devoted and skilled group joins forces with modern companions to speed up the supply of potential breakthrough medicines.

As we speak, our expansive oncology portfolio includes permitted and investigational remedies for a variety of blood cancers and stable tumors. We’re evaluating greater than 35 investigational medicines in a number of medical trials throughout a few of the world’s most widespread and debilitating cancers. As we work to have a exceptional influence on individuals’s lives, we’re dedicated to exploring options to assist sufferers get hold of entry to our most cancers medicines. For extra data, please go to http://www.abbvie.com/oncology .

Ahead-Wanting Statements
Some statements on this information launch are, or could also be thought-about, forward-looking statements for functions of the Personal Securities Litigation Reform Act of 1995. The phrases “imagine,” “anticipate,” “anticipate,” “venture” and comparable expressions and makes use of of future or conditional verbs, typically determine forward-looking statements. AbbVie cautions that these forward-looking statements are topic to dangers and uncertainties that will trigger precise outcomes to vary materially from these expressed or implied within the forward-looking statements. Such dangers and uncertainties embrace, however are usually not restricted to, challenges to mental property, competitors from different merchandise, difficulties inherent within the analysis and improvement course of, hostile litigation or authorities motion, modifications to legal guidelines and rules relevant to our business, the influence of world macroeconomic components, similar to financial downturns or uncertainty, worldwide battle, commerce disputes and tariffs, and different uncertainties and dangers related to world enterprise operations. Extra details about the financial, aggressive, governmental, technological and different components that will have an effect on AbbVie’s operations is ready forth in Merchandise 1A, “Threat Elements,” of AbbVie’s 2024 Annual Report on Type 10-Ok, which has been filed with the Securities and Change Fee, as up to date by its Quarterly Experiences on Type 10-Q and in different paperwork that AbbVie subsequently recordsdata with the Securities and Change Fee that replace, complement or supersede such data. AbbVie undertakes no obligation, and particularly declines, to launch publicly any revisions to forward-looking statements because of subsequent occasions or developments, besides as required by legislation.

References:

1. Camidge R, Raimbourg J, Lee Y-G, et al. Telisotuzumab Adizutecan (ABBV-400; Temab-A), a c-Met Protein-Concentrating on Antibody-Drug Conjugate, in Sufferers With Superior EGFR Mutated Non-Squamous NSCLC: Outcomes From a Section 1 Research. Summary 8512 offered on the American Society of Scientific Oncology Annual Assembly, 2025. Chicago, Illinois .
2. Cooper A, Chandana S, Furqan M, et al. Security and efficacy of ABBV-706, a seizure-related homolog protein (SEZ6)- concentrating on antibody-drug conjugate, in high-grade neuroendocrine neoplasms. Summary 105 offered on the American Society of Scientific Oncology Annual Assembly, 2025. Chicago, Illinois .
3. Sultana Q, Kar J, Verma A, et al. A Complete Evaluate on Neuroendocrine Neoplasms: Presentation, Pathophysiology and Administration. J Clin Med. 2023 Aug 5 ;12(15):5138. doi: 10.3390/jcm12155138.
4. Pemmaraju N, Marconi G, Montesinos P, et al. Efficacy and security of pivekimab sunirine (PVEK) in sufferers (pts) with blastic plasmacytoid dendritic cell neoplasm (BPDCN) within the CADENZA research. Summary 6502 offered on the American Society of Scientific Oncology Annual Assembly, 2025. Chicago, Illinois .
5. Cazzato G, Capuzzolo M, Bellitti E, et al. Blastic Plasmocytoid Dendritic Cell Neoplasm (BPDCN): Scientific Options and Histopathology with a Therapeutic Overview. Hematol Rep 2023;15(4):696-706 doi: 10.3390/hematolrep15040070.

Contacts:

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