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InkMune clinical trial goes on: second cohort is being treated
In phase 1/2 CaRe PC trial (NCT06056791) evaluating INKmune, a
biologic
therapy
In its announcement on Monday, INmune said it successfully completed nine INKmune administrations in the outpatient setting within the first cohort in the trial.
In phase 1/2 CaRe PC trial (NCT06056791) evaluating INKmune, a
biologic
therapy
In its announcement on Monday, INmune said it successfully completed nine INKmune administrations in the outpatient setting within the first cohort in the trial.
Maxone73
in
Advanced Prostate Cancer
2 months ago
new immune therapy phase 1-2 trial: targeting NK cells
The first patient with metastatic castration-resistant prostate cancer (mCRPC) has been dosed in the phase 1/2 CaRe PC trial (NCT06056791) evaluating INKmune, a
biologic
therapy
https://www.targetedonc.com/view/first-patient-dosed-with-inkmune-therapy-in-phase-1-2-trial-for-mcrpc
The first patient with metastatic castration-resistant prostate cancer (mCRPC) has been dosed in the phase 1/2 CaRe PC trial (NCT06056791) evaluating INKmune, a
biologic
therapy
https://www.targetedonc.com/view/first-patient-dosed-with-inkmune-therapy-in-phase-1-2-trial-for-mcrpc
Maxone73
in
Advanced Prostate Cancer
7 months ago
Biological Therapy - too soon?
Hey All I hope everyone is well. This is my first time posting and I’m really hopeful someone will be able to advise me. I was diagnosed with lupus in Feb after just over 2 years of struggling with symptoms. Initially I was put on prednisolone and hydroxychloroquine until my bloods came back. My bloods
Hey All I hope everyone is well. This is my first time posting and I’m really hopeful someone will be able to advise me. I was diagnosed with lupus in Feb after just over 2 years of struggling with symptoms. Initially I was put on prednisolone and hydroxychloroquine until my bloods came back. My bloods
EeBeee
in
LUPUS UK
4 days ago
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Change in inhalers
I'm currently on sertide and being switched over to symbicort. I'm not sure of the dosage etc as need to discuss further with gp. I'm a little concerned as been on seretide for years. When I get switched it triggers flares and I've already had loads of time of work. I work part time. I also think I'm
I'm currently on sertide and being switched over to symbicort. I'm not sure of the dosage etc as need to discuss further with gp. I'm a little concerned as been on seretide for years. When I get switched it triggers flares and I've already had loads of time of work. I work part time. I also think I'm
spookylou
in
Asthma Community Forum
3 months ago
No meds no symptoms
I was told a week ago to stop all my medication due to a chest infection and WBC being too low. I've been off my hydroxychloroquine and methotrexate for over a week now and weirdly my joints and swelling has been the best it's been for over 2 years. I feel perplexed has a 2 year flare just finished
I was told a week ago to stop all my medication due to a chest infection and WBC being too low. I've been off my hydroxychloroquine and methotrexate for over a week now and weirdly my joints and swelling has been the best it's been for over 2 years. I feel perplexed has a 2 year flare just finished
Sunshine634
in
LUPUS UK
3 months ago
Biological therapy.
I have been reading through all the posts on biological therapy.I have literally this week just heard that I qualify for Tezspire. The wait time is about 4 weeks. I am wondering who else is having this / had it and how they are getting on . Thank you.
I have been reading through all the posts on biological therapy.I have literally this week just heard that I qualify for Tezspire. The wait time is about 4 weeks. I am wondering who else is having this / had it and how they are getting on . Thank you.
pmrdec112014
in
Asthma Community Forum
4 months ago
biologic therapy blood tests to start Adalimumab
Hi after azaoprine caused liver cirrhosis, my consultant said I should start Adalimumab . I have had lots of various bloods taken including TB, HIV. Is this normal? 😳
Hi after azaoprine caused liver cirrhosis, my consultant said I should start Adalimumab . I have had lots of various bloods taken including TB, HIV. Is this normal? 😳
Bucket13
in
Crohn's and Colitis Support
1 year ago
biologic therapy
I have been on methotrexate for 20 years for RA. I started at 10 mg. Went to 15mg fairly promptly and then 20mg last year. In general I had no side effects and good quality of life. Recently I started to have a lot of flares and my rheumatologist has recommended a biologic. He said I could try upping
I have been on methotrexate for 20 years for RA. I started at 10 mg. Went to 15mg fairly promptly and then 20mg last year. In general I had no side effects and good quality of life. Recently I started to have a lot of flares and my rheumatologist has recommended a biologic. He said I could try upping
Barrcroom
in
NRAS
1 year ago
Greater use of Benlysta, Saphnelo seen in US, EU to treat lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
9 months ago
Biologic therapies
I am interested to know if anyone found the injection painful? My first was in the thigh and I am wondering if next time to try the arm or stomach area? Or am I just being a big baby?! 🫣
I am interested to know if anyone found the injection painful? My first was in the thigh and I am wondering if next time to try the arm or stomach area? Or am I just being a big baby?! 🫣
Headoverheels
in
Asthma Community Forum
1 year ago
consultant wants to reduce inhaler
I know it's likely I will need steroids again in the future without some type of
biologic
therapy
. My eosinophil count has been a bit raised during flare-ups (0.3) but not enough it seems to warrant any further therapy.
I know it's likely I will need steroids again in the future without some type of
biologic
therapy
. My eosinophil count has been a bit raised during flare-ups (0.3) but not enough it seems to warrant any further therapy.
ccccc
in
Asthma Community Forum
2 days ago
What is gene therapy and can it help people with Parkinson’s?
https://www.apdaparkinson.org/article/gene-therapy-for-parkinsons-disease-3/
https://www.apdaparkinson.org/article/gene-therapy-for-parkinsons-disease-3/
Farooqji
in
Cure Parkinson's
16 hours ago
Colomycin nebulising
I’m wondering if there is anyone on the above drug. I have been on it now for 10 days and will stay on it for 12 weeks. I have been pretty unwell since March with re occurring psuedamonas. I am on oxygen therapy, I also have bronciectasis and past T.B. also chicken pox pneumonia, I am on steroid therapy
I’m wondering if there is anyone on the above drug. I have been on it now for 10 days and will stay on it for 12 weeks. I have been pretty unwell since March with re occurring psuedamonas. I am on oxygen therapy, I also have bronciectasis and past T.B. also chicken pox pneumonia, I am on steroid therapy
breslin
in
Lung Conditions Community Forum
4 days ago
Klotho gene therapy
https://parkinsonsnewstoday.com/news/anew-medical-advance-development-klotho-gene-therapy/?utm_source=PAR&utm_campaign=c732d6332f-Email_ENL_US_PAR&utm_medium=email&utm_term=0_62dd4fb5e3-c732d6332f-74556474 I have been trying to find out what is used to prepare Klotho gene therapy a therapy that supposedly
https://parkinsonsnewstoday.com/news/anew-medical-advance-development-klotho-gene-therapy/?utm_source=PAR&utm_campaign=c732d6332f-Email_ENL_US_PAR&utm_medium=email&utm_term=0_62dd4fb5e3-c732d6332f-74556474 I have been trying to find out what is used to prepare Klotho gene therapy a therapy that supposedly
Boscoejean
in
Cure Parkinson's
5 days ago
Not dying was a good plan, but how to navigate the future is the next challenge
I appreciate that I have achieved remission with my cancer and I was thinking about the fact that my liver, even though I have cirrhosis, managed all of the chemo drugs I've had pretty successfully. In our patient groups we often see people who die quickly when a second problem appears. As a vote
I appreciate that I have achieved remission with my cancer and I was thinking about the fact that my liver, even though I have cirrhosis, managed all of the chemo drugs I've had pretty successfully. In our patient groups we often see people who die quickly when a second problem appears. As a vote
nash2
Partner
in
Living with Fatty Liver and NASH
5 days ago
Median PFS for FCR treated CLL patients with IGHV-M was 14.6 years vs 4.2 years for patients with IGHV-UM. V+O and I+R look to be superior
An update of the long-term follow-up results from the original 300-patient FCR (fludarabine, cyclophosphamide, and rituximab) study initiated at MD Anderson in 1999,
Sustained remissions in CLL after frontline FCR treatment with very-long-term follow-up,
reports ~47% of patients with mutated IGHV
An update of the long-term follow-up results from the original 300-patient FCR (fludarabine, cyclophosphamide, and rituximab) study initiated at MD Anderson in 1999,
Sustained remissions in CLL after frontline FCR treatment with very-long-term follow-up,
reports ~47% of patients with mutated IGHV
AussieNeil
Partner
in
CLL Support
6 days ago
Anybody outside the range part 2.
Hello again, the original post from yesterday and some more information and questions underneath. Thanks again for all the help. Part 1 Good afternoon everybody hope this makes sense Is there anybody out there that needs to run outside the ranges in order to feel good? At
Hello again, the original post from yesterday and some more information and questions underneath. Thanks again for all the help. Part 1 Good afternoon everybody hope this makes sense Is there anybody out there that needs to run outside the ranges in order to feel good? At
Jimjamio
in
Thyroid UK
6 days ago
ICU Stay Neuro Challenges
Seeing if anyone has any insight. On May 16th my mom (62 years old) went to her cardiologist with chest pain. She did have afib for the last three year but she had that under control. When she went to her cardiologist on the 16th he sent her to the ER just because he was concerned with chest pains
Seeing if anyone has any insight. On May 16th my mom (62 years old) went to her cardiologist with chest pain. She did have afib for the last three year but she had that under control. When she went to her cardiologist on the 16th he sent her to the ER just because he was concerned with chest pains
Doglover276
in
ICUsteps
7 days ago
Subcutaneous combination therapy improves ‘good on’ time in Parkinson’s
Primary analyses from this phase 3 clinical trial of the investigational, subcutaneous infusion of levodopa/carbidopa (LD/CD) (ND0612) showed that treatment in doses of up to 720 mg/90 mg per day, supplemented with oral levodopa provided almost 2 additional hours per day of “Good On” time without troublesome
Primary analyses from this phase 3 clinical trial of the investigational, subcutaneous infusion of levodopa/carbidopa (LD/CD) (ND0612) showed that treatment in doses of up to 720 mg/90 mg per day, supplemented with oral levodopa provided almost 2 additional hours per day of “Good On” time without troublesome
Farooqji
in
Cure Parkinson's
8 days ago
Med Trials - Tell me Your Experiences
We’re on the med journey that I’m sure so many of you know well. My son is 7.5 ASD/PDA, originally also diagnosed ADHD with lots of anxiety. He struggles big time with emotional regulation, aggression, following routines and demands. He’s extremely verbal and social but has a hard time making and keeping
We’re on the med journey that I’m sure so many of you know well. My son is 7.5 ASD/PDA, originally also diagnosed ADHD with lots of anxiety. He struggles big time with emotional regulation, aggression, following routines and demands. He’s extremely verbal and social but has a hard time making and keeping
STARTwHello
in
CHADD's ADHD Parents Together
8 days ago
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