Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Ligand Pharmaceuticals Inc. announces ZELSUVMI™ FDA approval for treating molluscum contagiosum in adults and children over 1 year old
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3 min read
Ligand Pharmaceuticals Inc. announces ZELSUVMI™ FDA approval for treating molluscum contagiosum in adults and children over 1 year old
10 January 2024
Ligand Pharmaceuticals Inc. has announced FDA approval for ZELSUVMI™ (berdazimer topical gel, 10.3%), now approved to treat molluscum contagiosum in adults and children aged 1 and older.
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BioPharma Accord, Inc. announces FDA approval for their STELARA® biosimilar, DMB-3115 license application
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3 min read
BioPharma Accord, Inc. announces FDA approval for their STELARA® biosimilar, DMB-3115 license application
10 January 2024
BioPharma Accord, Inc. reports the U.S. FDA has greenlit their application for a license regarding their proposed biosimilar to STELARA®, named DMB-3115.
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Innate Pharma's Lacutamab Clinical Program resumes with FDA's approval after lifting previous partial hold
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3 min read
Innate Pharma's Lacutamab Clinical Program resumes with FDA's approval after lifting previous partial hold
10 January 2024
Innate Pharma has been given the green light by the FDA to resume its Lacutamab Clinical Program after the previous partial clinical hold was removed.
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Why is it important to strictly follow the protocol of clinical trials?
Knowledge Base
2 min read
Why is it important to strictly follow the protocol of clinical trials?
10 January 2024
Now the new regulation stresses that the old version of the test documents should be kept and indicated with expiration date.
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Avenzo Therapeutics unveils promising CDK2 inhibitor AVZO-021, originally from Allorion Therapeutics
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3 min read
Avenzo Therapeutics unveils promising CDK2 inhibitor AVZO-021, originally from Allorion Therapeutics
10 January 2024
Avenzo Therapeutics has disclosed the promising clinical phase CDK2 inhibitor known as AVZO-021, originally developed by Allorion Therapeutics.
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Who should be responsible for the statistical analysis of clinical trials?
Knowledge Base
2 min read
Who should be responsible for the statistical analysis of clinical trials?
10 January 2024
Upon trial completion, the supervisor will retrieve the original case report form's first page, followed by data entry into the database for statistical analysis by the biostatistician per the pre-trial plan.
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Inspirna partners with German Merck KGaA to accelerate global development of RGX-202, also called Ompenaclid
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4 min read
Inspirna partners with German Merck KGaA to accelerate global development of RGX-202, also called Ompenaclid
9 January 2024
Inspirna teams up with German-based Merck KGaA to expedite the worldwide advancement of the drug Ompenaclid, known as RGX-202
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TLR9 agonists: What They Are and How to Stay Updated on the Latest Research
TLR9 agonists: What They Are and How to Stay Updated on the Latest Research
9 January 2024
TLR9 agonists are molecules that activate the Toll-like receptor 9, enhancing immune response against microbial infections.
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Debiopharm and Repare Therapeutics partner to explore combined PKMYT1 and WEE1 inhibitor use for cancer therapy
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3 min read
Debiopharm and Repare Therapeutics partner to explore combined PKMYT1 and WEE1 inhibitor use for cancer therapy
9 January 2024
Debiopharm is collaborating with Repare Therapeutics to investigate combining PKMYT1 and WEE1 inhibitors as a potential cancer treatment strategy.
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Can subjects voluntarily withdraw from clinical trials?
Knowledge Base
2 min read
Can subjects voluntarily withdraw from clinical trials?
9 January 2024
According to the tenets of the declaration of Helsinki, subjects can withdraw from the trial at any time according to their own wishes without any reason.
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D2 receptor antagonists: What They Are and How to Keep Up with the Latest Advances
D2 receptor antagonists: What They Are and How to Keep Up with the Latest Advances
9 January 2024
D2 receptor antagonists are drugs that block the D2 subtype of dopamine receptors, used in treating conditions like schizophrenia and bipolar disorder.
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Kyverna's KYV-101 has received FDA clearance for a Phase 2 trial, KYSA-7, for advanced Multiple Sclerosis patients resistant to other treatments
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3 min read
Kyverna's KYV-101 has received FDA clearance for a Phase 2 trial, KYSA-7, for advanced Multiple Sclerosis patients resistant to other treatments
9 January 2024
KYV-101, a therapeutic agent by Kyverna, has been granted approval by the American FDA for use in a Phase 2 study, KYSA-7, targeting individuals suffering from advanced, treatment-resistant Multiple Sclerosis.
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