Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma’s Nemluvio® Approved in EU for Atopic Dermatitis & Prurigo
Details : Nemluvio (nemolizumab) is a humanized anti-human IL-31 receptor A monoclonal antibody, approved for the treatment of patients with moderate-to-severe atopic dermatitis.
Product Name : Nemluvio
Product Type : Antibody
Upfront Cash : Inapplicable
February 14, 2025
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma’s Relfydess Shows Fast, Long-Lasting Aesthetic Results
Details : Relfydess (relabotulinumtoxinA) is the first and only ready-to-use liquid neuromodulator created with PEARL™ Technology for moderate to severe vertical frown lines.
Product Name : Relfydess
Product Type : Protein
Upfront Cash : Inapplicable
January 30, 2025
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
CHMP Recommends Nemolizumab Approval for Atopic Dermatitis and Prurigo Nodularis
Details : Nemluvio (nemolizumab) is a humanized anti-human IL-31 receptor A monoclonal antibody, approved for the treatment of patients with moderate-to-severe atopic dermatitis & prurigo nodularis.
Product Name : Nemluvio
Product Type : Antibody
Upfront Cash : Inapplicable
December 13, 2024
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma Gets FDA Approval for Nemluvio® for Moderate-To-Severe Atopic Dermatitis
Details : Nemluvio (nemolizumab) is a humanized anti-human IL-31 receptor A monoclonal antibody, approved for the treatment of patients with moderate-to-severe atopic dermatitis.
Product Name : Nemluvio
Product Type : Antibody
Upfront Cash : Inapplicable
December 13, 2024
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma Receives FDA Approval for Nemluvio® in Adults with Prurigo Nodularis
Details : Nemluvio (nemolizumab) is a humanized anti-human IL-31 receptor A monoclonal antibody, approved for the treatment of patients with prurigo nodularis.
Product Name : Nemluvio
Product Type : Antibody
Upfront Cash : Inapplicable
December 08, 2024
Lead Product(s) : Nemolizumab
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Phase III READY-4 Study Confirms Relfydess™ Safety in Long-Term Use
Details : Relfydess (relabotulinumtoxinA) is the first and only ready-to-use liquid neuromodulator created with PEARL™ Technology for moderate to severe vertical frown lines.
Product Name : Relfydess
Product Type : Protein
Upfront Cash : Inapplicable
October 21, 2024
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma’s Relfydess™ (RelabotulinumtoxinA) Receives Positive Decision for Use in Europe
Details : Relfydess (relabotulinumtoxinA) is the first and only ready-to-use liquid neuromodulator created with PEARL™ Technology for moderate to severe vertical frown lines.
Product Name : Relfydess
Product Type : Protein
Upfront Cash : Inapplicable
July 30, 2024
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Study Phase : Phase III
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Galderma’s Phase 3 Results Show Efficacy and Long Duration for Frown Lines and Crow's Feet
Details : QM1114-DP (relabotulinumtoxinA) is a botulinum toxin neuromodulator, which is under phase 3 clinical development for the treatment of glabellar frown lines & lateral canthal lines.
Product Name : Relfydess
Product Type : Protein
Upfront Cash : Inapplicable
January 16, 2024
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Highest Development Status : Phase III
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Study Phase : Phase III
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : QM1114-DP (RelabotulinumtoxinA) is a rapid and long lasting small molecule injection formulation, which is being investigated for dermatological conditions like Crow’s Feet and Frown Lines.
Product Name : Relfydess
Product Type : Protein
Upfront Cash : Inapplicable
November 30, 2023
Lead Product(s) : RelabotulinumtoxinA
Therapeutic Area : Dermatology
Highest Development Status : Phase III
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : L-Lactic Acid,Carboxymethyl Cellulose
Therapeutic Area : Dermatology
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Sculptra is the first and original injectable collagen stimulator containing microparticles of unique poly-L-lactic acid (PLLA-SCA) which gradually revitalizes the skin’s structural foundation.
Product Name : Sculptra
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
March 30, 2023
Lead Product(s) : L-Lactic Acid,Carboxymethyl Cellulose
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable