drug
teclistamab
Marketedupdated 5mo agoby Janssen Biotech Inc
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 3all catalysts(11)
approval · 11
Oct 25, 2022
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Aug 9, 2023
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Nov 16, 2023
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Feb 20, 2024
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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May 28, 2024
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Jul 2, 2024
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Nov 22, 2024
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Dec 2, 2024
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Aug 19, 2025
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Oct 2, 2025
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Mar 5, 2026
approval
TECVAYLI (TECLISTAMAB-CQYV) — FDA approval
teclistamab
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Trials studying teclistamab
- phase2Teclistamab In Waldenstrom's Macroglobulinemia
- phase3A Study Comparing JNJ-79635322 and an Anti-B-cell Maturation Antigen (BCMA)xCD3 Bispecific Antibody in Participants With Relapsed or Refractory Multiple Myeloma
- phase3A Study Comparing JNJ-79635322 and Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma
- phase1A Study of Teclistamab and Mezigdomide in People With Multiple Myeloma
- phase2A Phase II Study to Evaluate the Efficacy and Safety of Teclistamab in Combination With Daratumumab (Tec-Dara) in Newly Diagnosed Multiple Myeloma With Concurrent Light Chain Amyloidosis (MM+AL).
- phase3A Study Comparing Talquetamab Plus Pomalidomide, Talquetamab Plus Teclistamab, and Elotuzumab, Pomalidomide, and Dexamethasone or Pomalidomide, Bortezomib, and Dexamethasone in Participants With Relapsed or Refractory Myeloma Who Have Received an Anti-CD38 Antibody and Lenalidomide
- phase3A Study to Evaluate Adverse Events and Change in Disease Activity With Injected Etentamig Plus Oral Pomalidomide Versus Standard Therapies in Adults With Relapsed or Refractory Multiple Myeloma
- phase1A Study of Teclistamab With Other Anticancer Therapies in Participants With Multiple Myeloma
News(10)
- Novartis wagers almost $8B on a Chinese biotech’s RNA drugsIn exchange for a $575 million payment up front, Abogen Biosciences will furnish Novartis with access to its RNA technology, including an option to license its lead program ABO-2203.biopharma_dive · 4d ago
- Novartis bets up to $7.8B for an mRNA-encoded T cell engager from China’s AbogenNovartis is licensing an mRNA-based therapy designed to produce a CD3xCD19 T cell engager inside the body. Abogen Biosciences says the in vivo approach could reduce the likelihood of dangerous cyto…biospace · 4d ago
- GSK bags Chimagen’s trispecific T cell engager in deal worth up to $750MAfter inking a T cell engager pact with Chimagen Biosciences a few years ago, GSK is back for more, this time acquiring a multiple myeloma program from the antibody specialist.biospace · 21d ago
- GSK doubles down on Chimagen with $750M multiple myeloma wagerGSK has bet up to $750 million on a Chimagen Biosciences trispecific T-cell engager, positioning the Big Pharma to start phase 1 development of the multiple myeloma drug candidate next year. The de…fiercebiotech · 21d ago
- Trailing rivals, AbbVie scores win with dual-acting myeloma drugThe drugmaker is leaning on a better side effect profile compared to drugs from J&J, Pfizer and Regeneron as it pushes etentamig toward FDA submission.biopharma_dive · 1mo ago
- AbbVie’s T cell engager delivers survival benefit in Phase 3 multiple myeloma studyAbbVie’s etentamig has a relatively cleaner safety profile and an administration schedule that could give it an edge over other BCMA-targeting multiple myeloma therapies on the market, according to…biospace · 1mo ago
- AbbVie’s bispecific T-cell engager shows promise in ph. 3 multiple myeloma trialAbbVie released positive phase 3 data Thursday showing that its bispecific T-cell engager etentamig improved response rates and progression-free survival in patients with relapsed/refractory multip…fiercebiotech · 1mo ago
- Regeneron ends eye disease trial for anti-CD3 antibody following safety reviewRegeneron has hit the brakes on the phase 1/2a trial for an experimental eye inflammation treatment, following an adverse event that tilted the drug’s risk/benefit profile in the wrong direction.fiercebiotech · 1mo ago
- Lilly pens $370M deal with OmniAb for ion channel collab, but details remain vagueAntibody platform business OmniAb continues to rack up Big Pharma partnerships, with Eli Lilly signing off on up to $370 million biobucks tied to an ion channel program.fiercebiotech · 1mo ago
- Legend Biotech CEO abruptly steps down without permanent replacementIn a sudden leadership shift, Legend Biotech announced that its CEO, Ying Huang, Ph.D., resigned on Friday, with no permanent replacement yet named.fiercebiotech · 2mo ago
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