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AGTC Launches XLRP Gene Therapy Clinical Trial at Five Sites in U.S.

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Applied Genetic Technologies Corporation (AGTC) is now recruiting for its Phase 1/2 gene therapy clinical trial for males with X-linked retinitis pigmentosa (XLRP) caused by mutations in the gene RPGR. Approximately 15 patients will be enrolled in the study, which is primarily evaluating safety. Three doses of the gene therapy will be tested. The trial is taking place at five sites in the U.S.

“We are very pleased for this trial to begin enrolling patients,” says Stephen Rose, PhD, chief research officer, Foundation Fighting Blindness. “XLRP is a devastating retinal disease affecting about 15,000 people in the U.S. AGTC’s potential treatment provides real hope to those who are in desperate need of a vision-saving therapy.”

XLRP causes progressive and significant vision loss — namely night blindness and constriction of vision — in males. Usually diagnosed during childhood, XLRP often leads to legal blindness by age 45. While females are usually unaffected carriers of XLRP, they can have vision loss, as well

“We are deeply committed to advancing gene therapy to improve the lives of people with rare inherited retinal disorders that have no available treatments,” says Sue Washer, president and CEO of AGTC. “The initiation of the XLRP clinical trial brings us one step closer to bringing a potential treatment to affected individuals with the hope for restoring their vision.”

Three genes when mutated can cause XLRP. About 70 percent of cases are caused by mutations in the gene RPGR. AGTC’s emerging therapy is designed to help patients with any mutation in RPGR.

The Foundation Fighting Blindness funded canine studies at the University of Pennsylvania that showed XLRP (RPGR) gene therapy led to vision improvements sustained for at least 3.5 years.

AGTC’s XLRP gene therapy involves injection of healthy copies of RPGR underneath the retina. The RPGR copies are contained in a human-engineered virus — known as an adeno-associated virus or AAV — which is designed to readily penetrate retinal cells to deliver the therapeutic genetic cargo.

AGTC also has two gene therapy clinical trials underway for achromatopsia, a retinal condition which leads to vision loss and day blindness. One trial is for people with mutations in CNGA3. The other is for people with mutations in CNGB3.

The company also has a clinical trial ongoing for retinoschisis, which causes vision loss from splitting of retinal layers.

18 Responses to 'AGTC Launches XLRP Gene Therapy Clinical Trial at Five Sites in U.S.'

  1. Ahmad Basil Jenkins says:

    I would like to be a candidate for a trial for gene therapy. Please contact me, I would like to be involved. I’m a Preacher in Florida, and it would be a blessing to save any of my sight to preach his gospel.

  2. JO ANNE L. MENDES says:


  3. Zenda Shepherd says:

    Hi, my son and my nephew have RPGR X-link
    How can they get in on the trials? Both live in Nevada

  4. Mohd Ahmar says:

    Hello sir I m from India my
    wife is suffering from RP she is 28 years old and her condition is now worse day by day please suggest me how to enroll for these clinical trail. Any possibility to stop her vision loss for sometime.

    • EyeOnTheCure says:

      We are aware of the following clinics in India, which may be helpful:
      Shankara Netralaya, Chennai
      L. V. Prasad Eye Institute, Hyderabad – They have branches in different states
      Aravind Eye Hospital, Madhurai
      All India Institute of Medical Sciences- New Delhi

      If you are interested in a clinic in a different location, contact one of these clinics and ask them for a suggested clinic in your region.

  5. Jenny Falconer says:

    My husband has the exact disease . We having been watching closely what has been happening in England . We live in NZ .what are the chances of being able to be treated .

  6. Mary says:

    My sister has RP. Please please add her to your clinical trial. She is nearly blind.

  7. RUCHI AGRAWAL says:

    i have got rp my gene no 26 is effect as report done by me age 31 year female res india city mumbai interested in trial pl add my name

  8. Sumesh Nair says:

    Hi, We are from India but settled in Sharjah. I have my son being diagnosed with RP 1.5yrs back. He is of 7 yrs old. His condition has worsen in this shorter period and can’t read or write. I would like to know more details of the test. Is the test being targeted to a particular Gene or is it common for all RP patients. Really looking forward to hear from your team.

    • EyeOnTheCure says:

      Hi Sumesh, this clinical trials is for males with X-linked retinitis pigmentosa (XLRP) caused by mutations in the gene RPGR. Hope this helps!

  9. Mark Pearson says:

    I would like to be a part of this study but I am not sure what type of RP I have. How do I find out?

    • EyeOnTheCure says:

      Hi Mark, we recommend getting genetic testing to find out what is causing your RP. If you are interested in participating in FFB’s free genetic testing study, you need to first register on the Foundation’s free and secure patient registry at After you have registered, members can send an email to indicating your interest in genetic testing. Enrolling in My Retina Tracker is a good first step being notified of upcoming clinical trials as well. Hope this helps!

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