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OTC Industry News - Production & Manufacturing - Pharmaceutical Business Review
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Mannatech launches Uth Advanced Skin Matrix Rejuvenation Creme - Pharmaceutical Business Review
Mannatech, the founder of the Mission 5 Million social entrepreneurial movement and innovator of naturally-sourced supplements based on Real Food Tech
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Meda purchases MidNite OTC sleep aid - Pharmaceutical Business Review
Specialty pharmaceutical company Meda has purchased non-sedating over the counter (OTC) sleep aid, MidNite, in the US.
Otc.pharmaceutical-business-review.com news digest
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3 years
TFF Pharmaceuticals, Felix Biotechnology sign LOI for collaboration, development...
Under this proposed CDLA agreement, Felix Biotechnology would obtain a worldwide license to TFF Pharmaceuticals’ Thin Film Freezing technology to develop and manufacture dry powder formulations of a novel, bacteriophage-based biotherapeutics for inhalation...
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3 years
Merck to buy biopharmaceutical firm VelosBio for $2.75bn
Based in San Diego, VelosBio is involved in the development of first-in-class cancer therapies targeting receptor tyrosine kinase-like orphan receptor 1 (ROR1).
VLS-101, the company’s investigational antibody-drug conjugate (ADC) targeting ROR1, is currently being assessed in a phase I and a phase 2 clinical study to treat patients with haematologic malignancies and solid tumours.... -
3 years
NanOlogy enrols first patient in phase 2 trial of NanoPac for intratumoral treat...
The single arm trial is evaluating up to 3 monthly injections of the investigational drug in patients scheduled for prostatectomy approximately 90 days after the first injection.
Patients will be followed for safety and tumor response. Immune effects will be evaluated via multiplex immunohistochemistry and flow cytometry.... -
3 years
XNK Therapeutics receives US orphan drug status for NK cell-based immunotherapy ...
Receiving ODD status from the FDA for the treatment of multiple myeloma is a critical next step for the development of XNK’s leading investigational drug candidate. XNK has already received ODD status in the EU.
“Obtaining an ODD by the FDA is a significant milestone for XNK and our goal of taking the present drug candidate to the next level,” said Johan Liwing, CEO of XNK Therapeutics. “This is the starting point for us to expand clinical development into the...
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Web host: | Amazon Technologies Inc. |
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Updated: | April 03, 2024 |
Expires: | April 14, 2025 |
Created: | April 14, 2003 |
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