Sickle Cell Disease Insights

This week's must-know community updates, latest research & events

New This Week

Exciting news! There is now a new section featuring clinical trials that are actively recruiting patients. This highly requested addition gives you direct access to cutting-edge research opportunities that could shape the future of treatment.

Stay informed about potentially life-changing studies and let us know what you think by replying to this email!

Top Stories

Latest Research

In a comprehensive review by Pathology et al. (2025), the prevalence of alloimmunization in patients with sickle cell disease in the Middle East was found to be around 14%. Alloimmunization is a condition where the immune system reacts against foreign antigens after a blood transfusion. The study analyzed data from 19 studies including 3,867 patients. The most common antibodies developed were against the Kell, RhE, and RhD antigens, which are specific types of proteins on the surface of red blood cells.

The research also identified several risk factors for developing alloimmunization, such as being older, female, having a higher number of transfusions, and undergoing a splenectomy (removal of the spleen). Interestingly, the review highlighted that retrospective studies reported a higher prevalence of alloimmunization compared to cross-sectional studies. Pathology et al. emphasized the importance of matching blood transfusions not only for ABO and Rh types but also for the K antigen to reduce the risk of alloimmunization in patients with sickle cell disease.

Clinical Trials

This is a list of upcoming or ongoing clinical trials that are actively recruiting and have been listed or updated in the last two weeks:
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Oral GSK4172239D Compared With Placebo in Sickle Cell Disease Participants Aged 18 to 50 Years
Study Type
Phase I
Location
United States
Age Range
18 - 50 Years
Enrollment
40
Study to Evaluate the Safety and Tolerability of Escalating Doses of Fostamatinib in Subjects With Stable Sickle Cell Disease
Study Type
Phase I
Location
Maryland
Age Range
18 - 65 Years
Enrollment
25
Pharmacokinetics, Efficacy and Safety of Twice Daily Dosing Regimen of Hydroxycarbamide Dispersible Tablets in Children With Sickle Cell Disease
Study Type
Phase II
Location
2 countries
Age Range
9 Months - 11 Years
Enrollment
50
Telemedicine for Children With Sickle Cell Disease
Study Type
Interventional
Location
Indiana
Age Range
16+ Years
Enrollment
60

Community News

SCD Association of America, IncSCD Association of America, IncMar 10, 2025

March is Blood Clot Awareness Month. People with sickle cell disease are at a higher risk of developing serious blood than the general population. Clots can form in the legs, lungs and even the brain, leading to life-threatening complications like stroke or pulmonary embolism. The good news is that early detection and prevention can make a world of difference. If you or a loved one has sickle cell disease, take a moment to learn about the warning signs and proactive steps you can take to stay safe. Learn more: https://buff.ly/8xukuPO

SCD Association of America, Inc Post
Global Alliance of Sickle Cell Disease OrganizationsGlobal Alliance of Sickle Cell Disease OrganizationsMar 10, 2025

ALTERNATIVE OPTIONS FOR SICKLE CELL PAIN MANAGEMENT:

1. Acupuncture

2. Massage Therapy

3. Heat Therapy

4. Hydrotherapy

5. Mind-Body Therapies

6. Aromatherapy

7. Chiropractic Care

8. Nutritional Therapy

9. Mindfulness-Based Stress Reduction (MBSR)

Remember to consult with a healthcare professional before trying any new pain management techniques.

#SickleCellAwareness#GASCDO#EquityInCare#Advocacy#Strength#SickleCellWarriors#awareness#pain

Sick CellsSick CellsMar 12, 2025

It’s been a great day of Hill meetings! A huge thank you to all the advocates who showed up, shared their voices, and made an impact. Your dedication is truly inspiring!

Please keep tagging us and sharing your photos—we love seeing all the advocacy in action! 📸❤️

Sick Cells Post

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