US begins Stem cells Traisl for Hearing Loss in Infants

Cynthia

New member
US begins Stem cells Trials for Hearing Loss in Infants

WASHINGTON -- U.S. researchers have begun a groundbreaking trial to test the potential of umbilical cord blood transplants, a kind of stem cell therapy, to treat and possibly reverse hearing loss in infants.

The phase I trial follows promising studies on mice showing that such transplants were able to rebuild the structures of the inner ear, and some anecdotal evidence from humans, sparking hope of a cure for some forms of deafness.

One of those people is two-year-old Finn McGrath, who suffered brain damage after being deprived of oxygen during a prolonged and complicated delivery, according to his mother, Laura.

"His doctors told us he was at high risk for cerebral palsy, vision issues, hearing problems and mental retardation," she said in an interview with AFP.

Finn’s early days were an all-out struggle to survive, so for his parents, learning that he had failed his hearing tests and had damaged hair cells — the sensory receptors in the inner ear that pick up sounds — was almost an afterthought.

He had organ failure, breathing problems, and his cerebral palsy left him unable to roll, crawl or walk, hold his head up, talk or eat.

As his parents searched for ways to help him, they came upon stories online that told of studies using cord blood to help children with cerebral palsy and other disorders.

Prior to his birth, the McGraths had arranged to privately bank his umbilical cord blood, a procedure that costs around $2,000 plus storage fees, and remains controversial among pediatricians.

Private companies such as the Cord Blood Registry, which is funding the Texas study on hearing loss, urge expecting parents to bank their umbilical cord blood and reserve it for personal use as a way to protect their family.

That advice runs counter to the guidelines issues by the American Academy of Pediatrics in 2007, which calls such claims "unsubstantiated" and says banking for personal or family use "should be discouraged" but is "encouraged" if it is to be stored in a bank for public use.

Since Finn’s parents had already banked his, they enrolled him in cord blood trial for cerebral palsy in North Carolina and he received his first transplant in November 2009 when he was about seven weeks old.

A second transfusion followed and by May, his parents began to notice a change.

Nighttime noises, like an alarm on his food pump or the sound of ripping medical tape, would suddenly startle him awake, his mother recalled.

"He started vocalizing sounds and we could tell that he was anticipating things that we would say. Like, if he had heard a story a number of times or a song, he would smile like he recognized the song or the story."

Finn had a third infusion in September 2010, when he was one year old. Four months later, an otoacoustic emissions test (OAE), which plays a sound and picks up vibrations in the cochlea and hair cells, came back normal.

The early hearing tests that showed hearing loss were not exactly the same as the later tests that came back normal, so McGrath is cautious about comparing them directly, but she believes the cord blood transfusions may have helped.

"All I can tell you is anecdotally he was not able to hear for probably the first three or four months of his life, and then when he was about six to eight months old, he started hearing."

The hearing trial in Texas aims to take a first step in testing the safety, and later the efficacy, of transfusing cord blood in children age six weeks to 18 months who have sustained post-birth sensorineural hearing loss.

Some reasons that children lose their hearing at or after birth may include oxygen deprivation, head injury, infection, strong doses of antibiotics or loud noises.

Sensorineural hearing loss affects approximately six per 1,000 children, and there is no available medical treatment. Hearing aids or cochlear implants are typically offered to boost the ability of the damaged tissues.

"Stem cell therapy may potentially repair the damaged structures of the inner ear and restore normal hearing," lead investigator Samer Fakhri told AFP.

"We are at the initial stages of this process and the results are looking promising," Fakhri added.

Research using stem cells in cord blood, known as hematopoietic cells, is already under way on some types of brain injury, cerebral palsy, juvenile diabetes, kidney and lung disease, he said.

The new study at Memorial Hermann-Texas Medical Center is being funded by the Cord Blood Registry, and those eligible must have already banked their own umbilical cord blood with CBR.

But to Stephen Epstein, an otolaryngologist in Maryland, that does not pose a conflict of interest, because separate medical institutions in Texas and Georgia are conducting the Food and Drug Administration-approved research.

"If both of them can reproduce the same results then I would say it has some validity to it," said Epstein, who is not involved in the study.

"This is certainly a welcome, acceptable experiment, but it should be looked at with caution and time will tell."

One patient is already enrolled and the study, which runs for one year, has room for nine more.

While Finn McGrath still faces many challenges due to his cerebral palsy, his mother is grateful for the things he can do.

"I don’t know how much worse off he would have been without the stem cell transfusion," McGrath said, pointing to his normal cognition, lack of seizures, good hearing and vision.

"We remain hopeful that he will continue to improve."

© Copyright (c) AFP
 
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Harry

Member
Its great news, but its Phase 1, and if it is succesful which im sure it will be, the treatment will not be available to public for 5-10 years. i hope im wrong as my child has hearing loss and im desperate for her to be treated, but everytime i hear good news, it seems to always get delayed, not available for 10 years etc.

I dont know much about phase 1,2,3, but correct me if im wrong, i was told for a treatment to be FDA approved it has to go through at least phase 3 tests. If im wrong tell me, as im a bit a of Homer Simpson.
 

barbara

Pioneer Founding member
Four Phases of Clinical Studies in Humans
Phase 1 Trials
Clinical trials are organized into four categories, called phases. Phase 1 trials are primarily concerned with assessing the drug’s safety and tolerability and are the first step in testing new investigational medicines in humans. The patients in these trials usually number 20-100 and the trials may last several months. In addition to studying the investigational drug’s safety profile including the safe dosage range, these trials are designed to determine what happens to the investigational drug in the human body and how the investigational drug is absorbed, distributed, metabolized, excreted, and its duration of action. A Phase 1 trial will also investigate side effects that occur as dosage levels are increased. Except for drugs used to treat cancer, Phase 1 clinical trials are usually conducted in normal, healthy individuals and are not intended to treat (or prevent) disease or illness. Because cancer can be such a life-threatening condition, Phase 1 trials with anti-cancer drugs are usually carried out in patients who already have the disease.

Phase 2 Trials
Once a drug has been shown to be safe, it must still be tested for efficacy; that is, whether or not the experimental medicine has a desired effect on the targeted disease. Phase 2 trials are therapeutic studies to evaluate efficacy and to assess short-term safety of the study drug in patients suffering from a disease or condition for which the study drug is intended. This phase also determines appropriate dose ranges/regimens and, if possible, clarification of dose-response relationships to provide an optimal background for the design of larger therapeutic trials. Phase 2 trials are usually randomized, meaning that patients receiving treatment are divided between those that are administered the investigational drug, some that receive a comparable drug currently used to treat the targeted disease, and those that receive no drug (commonly referred to as placebo, an inactive substance that looks like the investigational drug). These trials are usually "blinded," a term used to describe that the researchers and patients are not aware of which group of patients is receiving the experimental drug and which group is not. The reason for "blinding the study" is to prevent bias from the researcher and patient when determining the effect experienced from the study medicines. In this manner, the trial can provide the investigators and the regulatory agency (e.g., FDA) comparative information about the relative safety of the new drug and its effectiveness. The number of patients in this phase of development typically ranges from 100 to 500 volunteer patients with disease. Typically, Phase 2 trials last from several months to up to 2 years.

Phase 3 Trials
Phase 3 trials, also referred to as registration or confirmatory trials, are designed to demonstrate efficacy and safety of the investigational drug or line extension in a larger population of patients with the disease that the drug is intended to treat. This requires large trials with patients who have the disease and involves comparing the investigational drug to comparator drugs and/or placebo. These trials usually enroll between 1,000 and 5,000 patients, last for 3 years or longer, and are conducted in a hospital or clinic setting. Physicians monitor the patients closely to confirm efficacy and identify adverse events from long-term use. Phase 3 trials provide evidence on whether a drug “works,” what dose should be used, what the risks of the molecule are, which patients may benefit from the therapy, and other information in determining whether the drug should be used in humans. Once Phase 3 trials are successfully completed, they are submitted to regulatory health agencies (e.g., FDA, European Medicines Agency [EMEA]) for review and possible marketing approval. Results of Phase 3 trials will determine the product labeling/prescribing information and how physicians are instructed to use the drug.

Phase 4 Trials
Phase 4 clinical trials are often called "post-marketing" trials because they begin after the Phase 1, 2, and 3 trial results have been given to the regulatory agency for review and marketing approval. Phase 4 trials usually enroll between several hundred to several thousand patients and may be designed to further evaluate safety in large populations; to determine if the drug is effective against other disease states; to test different ways of taking the drug such as tablets, time-release capsules, or syrups; and/or to determine the cost-effectiveness of the new drug relative to traditional other new therapies. Phase 4 trials typically occur throughout the life cycle of the approved medicine and are often required as a condition of marketing approval.
 

Cynthia

New member
Yes, it goods news and no it's not what we wish. There are clinics abroad that will treat hearing loss with no guarantees if you don't want to wait.

I think i read somewhere that Duke or University of North Carolina is now treating children with their cord blood for CP. Perhaps you could inquire if they would do more/
 
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