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“The information we’re presenting at this 12 months’s ASCO mirror the breadth and depth of our oncology pipeline and our unwavering dedication to analysis that might remodel outcomes for sufferers going through most cancers,” mentioned Roopal Thakkar , M.D., govt vp, analysis and growth and chief scientific officer, AbbVie. “These shows underscore our management in driving scientific innovation to deal with a number of the most urgent unmet wants in oncology right now by leveraging our modern platforms reminiscent of 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 development issue receptor (EGFR)-mutated non-squamous non-small cell lung most cancers (NSCLC) from the dose growth a part of a Section 1 research ( NCT05029882 ). ¹ Sufferers acquired a median of three prior strains 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 information cut-off, 54% of responders skilled a ≥6 months length of response (DoR). ¹ The commonest any-grade TEAEs in ≥30% of sufferers have been anemia (63%), nausea (61%), vomiting (37%), decreased urge for food (34%), and neutropenia (34%). ¹ Extra knowledge with 4 months follow-up shall be offered at ASCO.

  Temab-A can be being evaluated in a number of ongoing clinical trials together with a Section 1/2 Examine ( NCT06772623 ) in first-line NSCLC with out actionable genomic alterations together with budigalimab (AbbVie’s investigational programmed cell demise 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 strong tumors, acquired ABBV-706 monotherapy IV at 1.3–3.5 mg/kg as soon as each 3 weeks. ^2,3 Your entire cohort had an ORR of 31.3%, and a median DoR of 5.6 months. ² The commonest grade ≥3 TEAEs (cumulative throughout all dose ranges), have been anemia (45%), neutropenia (33%), and thrombocytopenia (21%). ² Extra knowledge shall 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 strong 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 have 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 shall be offered at ASCO.

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

“Over the previous few years, we have considerably expanded our ADC portfolio to research a broad vary of strong tumors and blood cancers, reflecting our deep dedication to remodeling most cancers care by focused therapies and biomarker pushed approaches,” mentioned Daejin Abidoye, M.D., vp, therapeutic space head of strong 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 info on AbbVie medical trials is obtainable 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 here .

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

Venetoclax, ibrutinib, epcoritamab, telisotuzumab vedotin are authorized medicines being investigated for added 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 tasks within the U.S. and Japan, with AbbVie accountable for additional international 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 exterior of the U.S.

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

U.S. Prescribing Data for AbbVie Medicines

Please see full Prescribing Information for EMRELIS ^™ (telisotuzumab vedotin-tllv)
Please see full Prescribing Information for EPKINLY ^® (epcoritamab-bysp)
Please see full Prescribing Information for IMBRUVICA ^® (ibrutinib)
Please see full Prescribing Information 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 now and tackle the medical challenges of tomorrow. We try to have a outstanding impression on folks’s lives throughout a number of key therapeutic areas together with immunology, oncology, neuroscience and eye care – and services in our Allergan Aesthetics portfolio. For extra details about AbbVie, please go to us at www.abbvie.com . Observe @abbvie on LinkedIn,   Facebook , Instagram , X (formerly 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 varieties in each blood cancers and strong 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 numerous, 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.

In the present day, our expansive oncology portfolio contains authorized and investigational therapies for a variety of blood cancers and strong tumors. We’re evaluating greater than 35 investigational medicines in a number of medical trials throughout a number of the world’s most widespread and debilitating cancers. As we work to have a outstanding impression on folks’s lives, we’re dedicated to exploring options to assist sufferers acquire entry to our most cancers medicines. For extra info, please go to http://www.abbvie.com/oncology .

Ahead-Trying 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 “consider,” “count on,” “anticipate,” “undertaking” and related 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 which will trigger precise outcomes to vary materially from these expressed or implied within the forward-looking statements. Such dangers and uncertainties embrace, however will not be restricted to, challenges to mental property, competitors from different merchandise, difficulties inherent within the analysis and growth course of, opposed litigation or authorities motion, modifications to legal guidelines and laws relevant to our business, the impression of world macroeconomic elements, reminiscent of financial downturns or uncertainty, worldwide battle, commerce disputes and tariffs, and different uncertainties and dangers related to international enterprise operations. Extra details about the financial, aggressive, governmental, technological and different elements which will have an effect on AbbVie’s operations is ready forth in Merchandise 1A, “Danger Elements,” of AbbVie’s 2024 Annual Report on Type 10-Ok, which has been filed with the Securities and Trade Fee, as up to date by its Quarterly Experiences on Type 10-Q and in different paperwork that AbbVie subsequently information with the Securities and Trade Fee that replace, complement or supersede such info. AbbVie undertakes no obligation, and particularly declines, to launch publicly any revisions to forward-looking statements on account 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 Examine. 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 Evaluation 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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