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Cellectis Provides Business Update and Reports 4th Quarter and Full Year 2020 Financial Results


Cellectis Provides Business Update and Reports 4th Quarter and Full Year 2020 Financial Results
March 04, 2021 16:42 ET
| Source:
Cellectis Inc.
Cellectis Inc.
New York, New York, UNITED STATES
Enrollment ongoing in 3 Cellectis-sponsored Phase 1 dose-escalation trials BALLI-01 in r/r B-ALL patients, AMELI-01 in r/r AML patients and MELANI-01 in r/r MM patients in 7 leading US clinical centers
Preliminary results from our Phase 1 BALLI-01 clinical study of UCART22 in adults with r/r B-ALL presented in oral session at 2020 ASH Annual Meeting
Partner Allogene Therapeutics presented initial results from Phase 1 ALPHA clinical study of licensed ALLO-501 in r/r NHL at 2020 ASCO Annual Meeting and from Phase 1 UNIVERSAL clinical study of licensed ALLO-715 in r/r MM at 2020 ASH Annual Meeting ....

United States , New York , France General , North Carolina , Stanford University , Stephan Grupp , Laurent Poirot , Philippe Duchateau , Cytovia Theraputics , Kyung Nam Wortman , Steve Doares , Iovance Biotherapeutics , Simon Harnest , Mark Frattini , Leopold Bertea , Iovance Biotherapeutic , Carrie Brownstein , Jean Pierre Garnier , Margaret Gandolfo , Conor Mcgoldrick , Head Of Information Technology , Calyxt Inc , American Society Of Clinical Oncology , Clinical Development Appointments , Louis Pasteur University Of Strasbourg , Delta Consulting Group ,

PCG Digital: Soligenix is Ready for Commercialization of SGX301 (HyBryte); FDA Has Approval Process on Fast Track


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New York, New York (Newsfile Corp. - February 23, 2021) - PCG Digital Operational efficiency and sound financial management lead to positive results. That statement sums up why Soligenix (NASDAQ: SNGX) is fast approaching a new drug application (NDA) submission and potential FDA approval for SGX301 (synthetic hypericin), a photodynamic treatment option to battle the debilitating effects of cutaneous T-Cell lymphoma (CTCL).
The most recent treatment option in their rare disease pipeline, SGX301, will potentially be known as HyBryte
following an FDA approval. Soligenix already has the key management and marketing plan in place for seamless commercialization, a rarity in the pharmaceutical world. ....

United States , New York , Christopher Schaber , York Newsfile Corp , Advisory Inc , Digital Holdings , Non Hodgkin Lymphoma , Vaccine Candidates , Pediatric Crohn , Radiation Enteritis , Digital Conference , Paid Advertising , Securities Act , ஒன்றுபட்டது மாநிலங்களில் , புதியது யார்க் , கிறிஸ்டோபர் ஸ்கேபர் , டிஜிட்டல் ஹோல்டிங்ஸ் , அல்லாத ஹாட்ஜ்கின் லிம்போமா , தடுப்பூசி வேட்பாளர்கள் , குழந்தை குரோன் , டிஜிட்டல் மாநாடு , பத்திரங்கள் நாடகம் ,

UKONIQ™ (umbralisib) Now Approved by the FDA; Onco360® Selected as Exclusive Specialty Pharmacy Partner


Press release content from Business Wire. The AP news staff was not involved in its creation.
UKONIQ™ (umbralisib) Now Approved by the FDA; Onco360® Selected as Exclusive Specialty Pharmacy Partner
February 8, 2021 GMT
LOUISVILLE, Ky. (BUSINESS WIRE) Feb 8, 2021
Onco360 ®, the nation’s largest independent Oncology Pharmacy, has been selected by TG Therapeutics, Inc. to be the exclusive specialty pharmacy partner for UKONIQ TM (umbralisib), a new oral treatment for adult patients with relapsed refractory marginal zone lymphoma who have received at least one prior anti-CD20-based regimen and relapsed refractory follicular lymphoma who have received at least three prior lines of systemic therapy. These indications are approved under accelerated approval based on overall response rate. Continued approval for these indications may be contingent upon verification and description of clinical benefit in a confirmatory trial. ....

United States , Benito Fernandez , Pharmerica Corporation , Tg Therapeutics Inc , Oncology Pharmacy , Chief Commercial Officer , Chief Commercial , Business Wire , Products And Services , Drug Approvals , Product Approvals , Consumer Products And Services , Diagnosis And Treatment , Health Care Industry , Non Hodgkin Lymphoma , Pharmacy Operators , New Products And Services , Medical Biotechnology Industry , Retail Industry , Corporate News , North America , Retail And Wholesale , Diseases And Conditions , Consumer Services , ஒன்றுபட்டது மாநிலங்களில் , பெனிட்டோ பெர்னாண்டஸ் ,

Immune dysregulation can affect the efficacy of CAR T therapy in some lymphoma patients


Immune dysregulation can affect the efficacy of CAR T therapy in some lymphoma patients
Chimeric antigen receptor T-cell therapy, or CAR T, has been a breakthrough in the treatment of blood cancers such as acute lymphoblastic leukemia and diffuse large B-cell lymphoma. Clinical studies have shown overall response rates of more than 80% with an ongoing response of nearly 40% more than two years after therapy. However, the cellular immunotherapy doesn t work for every patient.
Moffitt Cancer Center, one of the leading centers for cellular immunotherapy, is researching why some patients have a better CAR T response than others and what can be done to improve the treatment s effectiveness. In a new study published in ....

United States , Frederick Locke , Michael Jain , Emily Henderson , American Society Of Hematology , Cellular Immunotherapy Department At Moffitt , Oncology Program , Cellular Immunotherapy Department , Moffitt Cancer Center , Cancer Center , American Society , Vice Chair , Marrow Transplant , Immuno Oncology Program , Moffitt Cancer , Acute Lymphoblastic Leukemia , Chimeric Antigen Receptor , Hodgkin Lymphoma , Non Hodgkin Lymphoma , T Cell , ஒன்றுபட்டது மாநிலங்களில் , ஃப்ரெடரிக் பூட்டு , மைக்கேல் ஜெயின் , எமிலி ஹென்டர்சன் , அமெரிக்கன் சமூகம் ஆஃப் ஹீமாட்டாலஜி , செல்லுலார் நோயெதிர்ப்பு சிகிச்சை துறை இல் மாஃபிட் ,