GeneXp is our genetic testing system with an embedded software which can accurately analyse the rare and common genetic disorders. Our featured test is BRACA panel for breast cancer which strikes 22 million women in Pakistan at some point of their life, and PCSK9 test for familial hypercholesterolemia, which strikes 16 million people worldwide and 0.5 million people in Pakistan. 80% of people having this rare genetic condition are living without a diagnosis and experience early cardiovascular diseases such as stroke and heart attack.
Our Mission
At Cambridge GenetiX we believe in universal health services and giving importance to every single life. That’s why we have developed specialised tools for creating Human recombinant proteins, Biosimilar antibody drugs and a sophisticated genetic testing system for developing countries. These next generation therapies are designed meticulously by Scientists, Engineers and medical doctors from Harvard, Cambridge and Oxford universities paving a path to ensure better health worldwide. Our first drug Huminase is already accomplishing our mission.
Early detection of this variant can save millions of lives. GeneXp deals with 50 Genetic disorders including Cystic Fibrosis, Phenylketonuria, Haemophilia, Type 1Diabetes, sickle cell anaemia, Poly cystic kidney syndrome and many more.
Every year 33 million people suffer from stroke among them 21.6 million people are from developing countries such as Pakistan. Currently, stroke management is sub-standard and leads to high mortality rates. We are bringing a revolutionary stroke management product to the developing countries called Huminase.
Huminase is a recombinant from of Human plasminogen activator protein that destroys blood clots within hours of its administration after the stroke. Unlike streptokinase, Huminase can be used multiple time in an individual’s lifetime, immediately providing extra line of protection during re-occurrence of stroke.
Cambridge GenetiX is bringing 4th generation of advanced CAR-T cell lentivirus manufacturing services to facilitate clinicians who want to provide cell-based therapies to lymphoma cancer patients. In our proprietary system, we use a specially engineered vector system to produce high quality of viral particles which are ready to engineer patient derived T cells.
At Cambridge GenetiX we have prepared dozens of cell lines including MEFs, HeLa and HEK293T, which stably express inducible version of Cas9 enzymes under a GFP and puromycin selection markers. The cell lines come with a guide RNA cloning plasmid which allows your custom knockout to be a click away. Cambridge GenetiX cell lines allow you to perform a complete gene-knockout experiment in as little as 6 weeks. We are posting a complete list of CRISPR cell lines on our website soon.
hTERT immortalization system is one step solution provided by Cambridge GenetiX to immortalize your precious collection of patient-derived primary cell cultures. Normal cells divide for 9-10 passages before acquiring senescence. Collection of samples from multiple patients may introduce variability hence impacting your final results. Here we provide Lenti-virus particles which can introduce human Telomerase enzyme. hTERT is an enzyme which elongates the life of primary cell cultures from 10-60 passages, providing you enough material and confidence of reproducibility.
Origins
Cambridge GenetiX originates from a Nobel Prize winning Lab at Cambridge. Prof. J.B. Gurdon’s lab has mentored Lawrence J.Korn (Founder of Protein Design lnc.) and Douglas A. Melton (Co-Founder of Gilead and Founder Semma Therapeutics). Both companies have changed medicine by bringing blockbuster drugs like Herceptin and Avastin to patients. Semma therapeutics has brought a historical Stem Cell Therapy for Type-1-Diabetes. We hope to follow in the footsteps of companies like this who bought life changing treatments to patients through truly innovative and groundbreaking science.
Our Scientific Advisory Board
Leadership
Nowadays, Andy is still at the Gurdon Institute and is a member of the Cancer Research UK Cambridge Centre. He has spent the last three decades generally messing around with chromatin with a special focus on histones and their modifications. He has made several seminal contributions to the field, in which he is highly cited with a h-index of 59. More recently, his focus switched to the analysis of post-transcriptional RNA modifications and biochemical characterisation of the relevant enzymes. Throughout his career, Andy has warmly welcomed collaborative studies particularly with pharmaceutical companies, both large and small, and he has acted as a scientific consultant to many of these
Scientific Team
In 2019, she earned a BA Hons. in Human, Social and Political Sciences at Gonville and Caius College, Cambridge University, developing a special focus on health policy and medical ethics. She is currently completing an MSc Translational Medicine at the University of Helsinki in regenerative medicine and infectious diseases. Her research primarily centres around the use of neurotrophic factors in Parkinson’s disease and ALS, enhancing wound healing, and an interest in leveraging stem cells more broadly.
Zsofia has spent two years in Switzerland working with the GAVI Vaccine Alliance, WHO and UNAIDS on partnerships and policy coordination for routine immunisation programmes, COVID-19 vaccine distribution, and HIV/AIDS innovations. She has previously worked for ADDMedica, a Paris-based orphan sickle cell drug manufacturer, and holds a health reporting fellowship at Health Policy Watch.
Functional Team
Bilal brings his curiosity and resourcefulness to CamGentix where he is working very closely with the core functional team to bring ground-breaking healthcare to the developing world. Bilal works as an operational head in our GeneXp software and manages logistics and operations of Cambridge GenetiX.