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BioWorld - Sunday, May 10, 2026
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Regulatory front for June 30, 2020

June 30, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for June 30, 2020

June 30, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alterity, Ardelyx, Astrazeneca, Bioinvent, Mediwound, Merck, Nuvox, Oncopeptides, Oncternal, Osmotica, Prestige, Sparingvision, Synthetic Biologics, Vericel, Verrica.
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FDA approves Phesgo for HER2-positive breast cancer

June 30, 2020

Vadadustat approved in Japan for the treatment of anemia due to CKD

June 30, 2020

Onoact approved for additional indication of tachyarrhythmia associated with sepsis in Japan

June 30, 2020

Enspryng approved in Japan for adults and children with NMOSD

June 30, 2020
Product images of Acclaim models 9000 and 9200

FDA grants breakthrough status to Envoy Medical’s Acclaim cochlear implant

June 29, 2020
By Meg Bryant
Envoy Medical Corp. got some early support for its Acclaim fully implantable cochlear implant, with a breakthrough device designation from the U.S. FDA. If approved, it would be the first cochlear implant to address hearing loss without the use of any external components.
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Regulatory front for June 29, 2020

June 29, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: ACLA, I-Fixit, MITA, Palmetto GBA.
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Regulatory actions for June 29, 2020

June 29, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Beckman Coulter, Boston Scientific, Envoy Medical, Orthofix.
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FDA Not Approved stamp

Heron knocked by second CRL for postoperative pain drug

June 29, 2020
By Randy Osborne
Shares of Heron Therapeutics Inc. sank 27% in morning trading, after the San Diego-based firm disclosed a second complete response letter (CRL) for HTX-011 in postoperative pain. The CRL, received from the FDA on June 26, the anticipated PDUFA date, stated the agency was unable to approve the NDA in its present form and called for additional nonclinical information.
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