approval
saveACTEMRA (TOCILIZUMAB) — FDA approval
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Sponsor: GENENTECH. Form: INJECTABLE. Route: INJECTION
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drug timeline · 8
- phase 1 completionChugai Pharmaceutical Co Ltd — tocilizumab (Phase I Trial Completion)Apr 30, 2026 · 154d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalDec 10, 2025 · 295d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalDec 10, 2025 · 295d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalAug 8, 2025 · 419d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalDec 10, 2024 · 660d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalDec 10, 2024 · 660d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalSep 20, 2024 · 741d ago
- approvalACTEMRA (TOCILIZUMAB) — FDA approvalSep 20, 2024 · 741d ago
same company · ±60 days · 6
- approvaltocilizumab: ACTEMRA (TOCILIZUMAB) — FDA approvalAug 8, 2025
- approvalatezolizumab: TECENTRIQ (ATEZOLIZUMAB) — FDA approvalAug 18, 2025
- approval(atezolizumab + hyaluronidase (human recombinant)): TECENTRIQ HYBREZA (ATEZOLIZUMAB AND HYALURONIDASE-TQJS) — FDA approvalAug 18, 2025
- approvalinavolisib: ITOVEBI (INAVOLISIB) — FDA approvalSep 25, 2025
- approval(atezolizumab + hyaluronidase (human recombinant)): TECENTRIQ HYBREZA (ATEZOLIZUMAB AND HYALURONIDASE-TQJS) — FDA approvalOct 2, 2025
- approvalatezolizumab: TECENTRIQ (ATEZOLIZUMAB) — FDA approvalOct 2, 2025
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- companyCelltrion Inc4 co-mentions · 4 sources
- companyChugai Pharmaceutical Co Ltd1 co-mentions · 1 sources
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