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European Commission Grants Orphan Drug Designation to Loncastuximab Tesirine

The European Commission has granted Orphan Drug Designation to loncastuximab tesirine (Zynlonta®; ADC Therapeutics); previously known as ADCT-402, a CD19-targeted ADC, for the treatment...

Results of LOTIS-2 Study of Loncastuximab Tesirine Shows Substantial Single-agent Activity,...

Results of LOTIS-2, a multicenter, open-label, single-arm Phase II clinical trial evaluating the safety and efficacy of single-agent loncastuximab tesirine-lpyl (Zynlonta™; ADC Therapeutics; previously...

Withdrawal of FDA’s Accelerate Approved Therapeutic Agents may harm Patients

The United States Food and Drug Administration’s (FDA) program to accelerate approval of some promising therapeutic agents has recently come under fire due to...
ADC Biotechnology in Deeside, North-Wales, UK. With the availability of a new cleanroom, the company continues its focus on antibody-drug conjugates (ADCs) and developing new process technologies to speed up, simplify and significantly lower the production costs of the latest generation of anticancer blockbuster drugs.

Sterling Pharma Solutions Acquires ADC Biotechnology

Global contract development and manufacturing organization (CDMO), Sterling Pharma Solutions, has announced the acquisition of ADC Biotechnology, a UK-based bioconjugation development services business specializing...

FDA Approves Loncastuximab Tesirine in Treatment of Relapsed or Refractory Diffuse...

Diffuse large B-cell lymphoma (DLBCL), a form of non-Hodgkin lymphoma, is the most common form of blood cancer. Lymphomas occur when cells of the...

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