News about "CuraTeQ Biologics"

CuraTeQ Biologics Announces Positive Phase 3 Results for BP11, Biosimilar to Xolair

CuraTeQ Biologics Announces Positive Phase 3 Results for BP11, Biosimilar to Xolair

CuraTeQ Biologics reports positive Phase 3 results for BP11, a biosimilar to Xolair, meeting primary endpoints in Chronic Spontaneous Urticaria (CSU) studies across Europe and India.

CuraTeQ Biologics | 07/04/2026 | By News Bureau

Aurobindo's Subsidiary CuraTeQ Biologics Completes Phase 3 Clinical Study for Denosumab Biosimilar

Aurobindo's Subsidiary CuraTeQ Biologics Completes Phase 3 Clinical Study for Denosumab Biosimilar

CuraTeQ Biologics, a wholly owned subsidiary of Aurobindo Pharma, has successfully completed a pivotal clinical study of its denosumab biosimilar, evaluated against Amgen’s Prolia in 446 women with postmenopausal osteoporosis.

CuraTeQ Biologics | 19/09/2025 | By Dineshwori 342

CuraTeQ Biologics Receives UK MHRA Approval for Trastuzumab Biosimilar Dazublys

CuraTeQ Biologics Receives UK MHRA Approval for Trastuzumab Biosimilar Dazublys

CuraTeQ Biologics, a wholly owned step-down subsidiary of Aurobindo Pharma, has obtained marketing authorisation from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) for its trastuzumab biosimilar, Dazublys.

CuraTeQ Biologics | 26/08/2025 | By Dineshwori 255

CuraTeQ Biologics Secures UK MHRA Approval for Bevqolva

CuraTeQ Biologics Secures UK MHRA Approval for Bevqolva

Bevqolva 25 mg/mL concentrate for infusion will be available in 4 mL (100 mg) and 16 mL (400 mg) single-use vials for infusion into veins.

CuraTeQ Biologics | 23/12/2024 | By Aishwarya 630

Aurobindo Pharma Ltd's subsidiary to withdraw application for EU Marketing Authorization of two biosimilars

Aurobindo Pharma Ltd's subsidiary to withdraw application for EU Marketing Authorization of two biosimilars

Aurobindo Pharma Ltd's subsidiary to withdraw application for EU Marketing Authorization of two biosimilars

CuraTeQ Biologics | 26/06/2023 | By Sudeep Soparkar 1004


 

 

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