CELL AND GENE THERAPY INSIGHTS

Looking to a future of multiplex cell engineering

Looking to a future of multiplex cell engineering

Marco Alessandrini
11 January 2024
Interview
Exploring the burgeoning role of non-viral approaches in the delivery of nucleic acids

Exploring the burgeoning role of non-viral approaches in the delivery of nucleic acids

Zhenghong Gao
05 January 2024
Interview
Advancing multiplex base editing into the clinic

Advancing multiplex base editing into the clinic

Gopi Shanker
10 November 2023
Interview
Exploring the convergence of gene editing and RNAi in iPSC-derived allogeneic cell therapy

Exploring the convergence of gene editing and RNAi in iPSC-derived allogeneic cell therapy

Vlad Seitan
08 November 2023
Interview
Developing a multiplex gene editing approach targeting viral infection

Developing a multiplex gene editing approach targeting viral infection

TJ Cradick
08 November 2023
Interview
Bringing the Sleeping Beauty transposon system to the clinic

Bringing the Sleeping Beauty transposon system to the clinic

Zoltán Ivics
18 October 2023
Interview
Developing universal AAV immuno-gene therapy for oncology

Developing universal AAV immuno-gene therapy for oncology

Nicole Paulk
24 August 2023
Interview
Does synthetic biology hold the key to unlocking solid tumors for cell and gene therapy?

Does synthetic biology hold the key to unlocking solid tumors for cell and gene therapy?

Ming-Ru Wu
21 August 2023
Interview
Rearming the immune system with personalized allogeneic CAR-T cell therapy

Rearming the immune system with personalized allogeneic CAR-T cell therapy

Olivier Negre
18 August 2023
Interview
Exploring current shortfalls and potential improvements for non-viral gene delivery in cystic fibrosis

Exploring current shortfalls and potential improvements for non-viral gene delivery in cystic fibrosis

Uta Griesenbach
05 August 2023
Interview
Developing non-viral delivery & cell engineering technologies for ex vivo T cell immunotherapies

Developing non-viral delivery & cell engineering technologies for ex vivo T cell immunotherapies

Julie Shi, Nirveek Bhattacharjee
30 June 2023
Interview
Expanding the potential of in vivo cell therapy with tLNP-RNAs (targeted lipid nanoparticle-RNA)

Expanding the potential of in vivo cell therapy with tLNP-RNAs (targeted lipid nanoparticle-RNA)

Adrian Bot
28 June 2023
Interview
At the cutting edge of AAV capsid engineering

At the cutting edge of AAV capsid engineering

Eric Kelsic, Adrian Veres
31 May 2023
Interview
Utilizing AI to drive AAV-based gene delivery to the CNS

Utilizing AI to drive AAV-based gene delivery to the CNS

David Huss
31 May 2023
Interview
Assessing recent milestones in AAV capsid discovery & development for CNS applications

Assessing recent milestones in AAV capsid discovery & development for CNS applications

Mathieu Nonnenmacher
09 May 2023
Interview
Leveraging derisked AAV vector development & delivery approaches to enhance speed to market for rare disease gene therapies

Leveraging derisked AAV vector development & delivery approaches to enhance speed to market for rare disease gene therapies

Adrien Lemoine
28 April 2023
Interview
Navigating the path to clinic for ATMPs: a regulator’s perspective

Navigating the path to clinic for ATMPs: a regulator’s perspective

James W McBlane
02 February 2023
Interview
Leveraging cellular immunotherapy at the cutting edge of autoimmune disease R&D

Leveraging cellular immunotherapy at the cutting edge of autoimmune disease R&D

Silvio Manfredo-Vieira
12 December 2022
Interview
Advancing genome edited allogeneic cell therapies into the clinic

Advancing genome edited allogeneic cell therapies into the clinic

Steve Kanner
26 August 2022
Interview
Ensuring commercial readiness in the cellular cancer immunotherapy space

Ensuring commercial readiness in the cellular cancer immunotherapy space

Julian Adams, Michele Korfin, Ronit Simantov
16 August 2022
Interview
Driving stem cell innovation

Driving stem cell innovation

Brock Reeve
27 May 2022
Interview