Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Study Phase : Phase I/ Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
ReCode’s RCT2100 Gains FDA Orphan Drug Status for Cystic Fibrosis
Details : RCT2100 is an inhaled mRNA-based therapy developed using our novel SORT lipid nanoparticle delivery platform. It is being developed for the treatment of cystic fibrosis.
Product Name : RCT2100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
March 25, 2025
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Highest Development Status : Phase I/ Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Undisclosed
Therapeutic Area : Genetic Disease
Study Phase : Preclinical
Sponsor : Cystic Fibrosis Foundation
Deal Size : $15.0 million
Deal Type : Funding
ReCode Receives Cystic Fibrosis Foundation Funding for Gene Correction Therapies
Details : The proceeds will be used to accelerate ReCode’s gene correction research program with the goal of developing and commercializing new treatments for people with cystic fibrosis.
Product Name : Undisclosed
Product Type : Undisclosed
Upfront Cash : Undisclosed
November 18, 2024
Lead Product(s) : Undisclosed
Therapeutic Area : Genetic Disease
Highest Development Status : Preclinical
Sponsor : Cystic Fibrosis Foundation
Deal Size : $15.0 million
Deal Type : Funding
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Study Phase : Phase I/ Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
ReCode Doses First Patient in Phase 1b Study Of RCT2100 For Cystic Fibrosis
Details : RCT2100 is an investigational inhaled mRNA therapy, which is currently being evaluated for the treatment of patients with cystic fibrosis.
Product Name : RCT2100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
September 26, 2024
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Highest Development Status : Phase I/ Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
ReCode Receives FDA Orphan Drug Designation for RCT1100 in Primary Ciliary Dyskinesia
Details : RCT1100 is an inhaled mRNA therapy designed to deliver and express DNAI1 mRNA in target cells. It is under phase 1 clinical development for the treatment of Primary Ciliary Dyskinesia.
Product Name : RCT1100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
June 27, 2024
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
ReCode Doses First Patient in Phase 1 of mRNA Therapy for Primary Ciliary Dyskinesia
Details : RCT1100 is an inhaled mRNA therapy designed to deliver and express DNAI1 mRNA in target cells. It is under phase 1 clinical development for the treatment of Primary Ciliary Dyskinesia.
Product Name : RCT1100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
March 01, 2024
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Study Phase : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
ReCode Doses First Participants in Phase 1 Study of Inhaled mRNA for Cystic Fibrosis
Details : RCT2100 is an inhaled mRNA-based therapy developed using our novel SORT lipid nanoparticle delivery platform. It is being developed for the treatment of cystic fibrosis.
Product Name : RCT2100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
February 21, 2024
Lead Product(s) : RCT2100
Therapeutic Area : Genetic Disease
Highest Development Status : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : ARCT-032
Therapeutic Area : Genetic Disease
Study Phase : Preclinical
Sponsor : The Cystic Fibrosis Foundation
Deal Size : $15.0 million
Deal Type : Funding
Details : ReCode is developing an inhaled ARCT-032 (mRNA therapy), designed to provide a correct copy of the cystic fibrosis transmembrane conductance regulator (CFTR) mRNA to lung cells to make a functional CFTR protein.
Product Name : ARCT-032
Product Type : Oligonucleotide
Upfront Cash : Undisclosed
October 01, 2023
Lead Product(s) : ARCT-032
Therapeutic Area : Genetic Disease
Highest Development Status : Preclinical
Sponsor : The Cystic Fibrosis Foundation
Deal Size : $15.0 million
Deal Type : Funding
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase I
Sponsor : Bioluminescence Ventures
Deal Size : $260.0 million
Deal Type : Series B Financing
ReCode Therapeutics Announces Closing of Extension to Series B Financing
Details : The proceeds will advance ReCode’s proprietary Selective Organ Targeting lipid nanoparticle pipeline, including Phase 1 trial of RCT1100 for primary ciliary dyskinesia and RCT2100, its cystic fibrosis candidate.
Product Name : RCT1100
Product Type : Oligonucleotide
Upfront Cash : Undisclosed
September 19, 2023
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase I
Sponsor : Bioluminescence Ventures
Deal Size : $260.0 million
Deal Type : Series B Financing
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : RCT1100 is a first-in-class, mRNA-based genetic medicine for the treatment of people with primary ciliary dyskinesia (PCD) caused by pathogenic mutations in the DNAI1 gene that encodes a protein essential for ciliary movement.
Product Name : RCT1100
Product Type : Oligonucleotide
Upfront Cash : Inapplicable
March 15, 2023
Lead Product(s) : RCT1100
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase I
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Undisclosed
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Preclinical
Sponsor : Leaps by Bayer
Deal Size : $200.0 million
Deal Type : Series B Financing
Details : Proceeds from the financing will be used to fund the diversification of ReCode’s pipeline into central nervous system, liver, and oncology indications, while continuing to advance lead mRNA programs for primary ciliary dyskinesia and cystic fibrosis in...
Product Name : Undisclosed
Product Type : Oligonucleotide
Upfront Cash : Undisclosed
June 29, 2022
Lead Product(s) : Undisclosed
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Preclinical
Sponsor : Leaps by Bayer
Deal Size : $200.0 million
Deal Type : Series B Financing