Lori Ellis Head of Insights | Biospace
+ Pharmaceuticals
Patient Daily | Jun 2, 2026

Merck’s TROP2 strategy draws attention at ASCO as Keytruda faces future competition

Merck attracted analyst attention at the American Society of Clinical Oncology meeting in Chicago, where its ongoing efforts to build a post-Keytruda oncology portfolio were highlighted on June 2. While emerging biotechs like Revolution Medicines and Summit Therapeutics received significant media coverage during the event, analysts identified Merck as a potential key winner due to progress with its TROP2-directed therapies.

BMO Capital Markets said, “[The] ASCO event highlights the developmental progress Merck has made in oncology with efforts finally starting to pay off.” Data from the Phase 3 OptiTROP-Lung05 trial presented at ASCO showed an overall survival rate of 80.4% among Chinese patients with first-line non-small cell lung cancer treated with sacituzumab tirumotecan (sac-TMT), an antibody-drug conjugate targeting TROP2.

Despite these results, Merck’s shares declined amid interest in new PD-1/VEGF treatments showcased by other companies. BMO wrote, “While we think PD-(L)1/VEGF (specifically BNTX/BMY’s pumitamig) development has shown meaningful mechanistic validation this weekend, we come away feeling as if Merck’s TROP2 and potential for combinations with its own PD-1/VEGF could offer the company the firepower and trial flexibility to not only be a leader in NSCLC but other solid tumors with more readouts imminent.”

Analysts noted that although Merck is trailing competitors such as Summit and Akeso in the PD-1/VEGF race—its candidate MK-2010 is still early-stage—the company has demonstrated an ability to adapt quickly. Guggenheim analysts wrote, “While behind, we believe MRK has a history of learning from competitors and moving quickly and aggressively with programs where they see a meaningful opportunity, and they can leverage their combination of assets (MK-2010, sac-TMT, and more) to catch up.”

Looking ahead, Merck plans multiple clinical readouts for sac-TMT across several cancer types over the next three years. According to Guggenheim analysts, data from 16 Phase 3 trials will be released during this period. The company also aims to expand into hematology following its $6.7 billion acquisition of Terns Pharmaceuticals earlier this year.

Guggenheim concluded: “Overall…we believe Merck continues to do a commendable job in working to diversify away from Keytruda (both in and outside of oncology), highlighted by ~60 ongoing Phase 3 studies across their late-stage oncology pipeline and registrational readouts expected from 10 different assets in the next four years.”

Organizations in this story