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    [{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"MPM Capital","pharmaFlowCategory":"D","therapeuticArea":"Genetic Disease","country":"U.S.A","productType":"Large molecule","year":"2020","type":"Series A Financing","leadProduct":"mRNA-mediated protein replacement therapies","moa":"","graph1":"Genetic Disease","graph2":"Undisclosed","graph3":"ReCode Therapeutics","amount2":0.080000000000000002,"highestDevelopmentShortName":"Undisclosed","therapeuticAreaShortName":"Genetic Disease","amount2New":0.080000000000000002,"dosageForm":"","sponsorNew":"ReCode Therapeutics \/ MPM Capital","highestDevelopmentStatusID":"1","companyTruncated":"ReCode Therapeutics \/ MPM Capital"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","therapeuticArea":"Genetic Disease","country":"","productType":"Large molecule","year":"2021","type":"Not Applicable","leadProduct":"RNA-based therapy","moa":"CFTR gene","graph1":"Genetic 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Therapeutics","amount2":0.20000000000000001,"highestDevelopmentShortName":"Preclinical","therapeuticAreaShortName":"Rare Diseases","amount2New":0.20000000000000001,"dosageForm":"Aerosol","sponsorNew":"ReCode Therapeutics \/ Leaps by Bayer","highestDevelopmentStatusID":"4","companyTruncated":"ReCode Therapeutics \/ Leaps by Bayer"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"AskBio","pharmaFlowCategory":"D","therapeuticArea":"Technology","country":"","productType":"Cell and Gene therapy","year":"2023","type":"Collaboration","leadProduct":"Undisclosed","moa":"","graph1":"Technology","graph2":"Discovery Platform","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"Discovery Platform","therapeuticAreaShortName":"Technology","amount2New":0,"dosageForm":"","sponsorNew":"ReCode Therapeutics \/ ReCode Therapeutics","highestDevelopmentStatusID":"3","companyTruncated":"ReCode Therapeutics \/ ReCode Therapeutics"},{"orgOrder":0,"company":"ReCode 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Bioluminescence Ventures"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","therapeuticArea":"Rare Diseases and Disorders","country":"","productType":"Large molecule","year":"2024","type":"Not Applicable","leadProduct":"RCT1100","moa":"","graph1":"Rare Diseases and Disorders","graph2":"Phase I","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"Ph I","therapeuticAreaShortName":"Rare Diseases","amount2New":0,"dosageForm":"Inhalation Solution","sponsorNew":"ReCode Therapeutics \/ Not Applicable","highestDevelopmentStatusID":"6","companyTruncated":"ReCode Therapeutics \/ Not Applicable"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Intellia Therapeutics","pharmaFlowCategory":"D","therapeuticArea":"Genetic Disease","country":"","productType":"Cell and Gene therapy","year":"2024","type":"Collaboration","leadProduct":"CRISPR-based Therapy","moa":"","graph1":"Genetic Disease","graph2":"Discovery Platform","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"Discovery Platform","therapeuticAreaShortName":"Genetic Disease","amount2New":0,"dosageForm":"","sponsorNew":"ReCode Therapeutics \/ ReCode Therapeutics","highestDevelopmentStatusID":"3","companyTruncated":"ReCode Therapeutics \/ ReCode Therapeutics"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","therapeuticArea":"Genetic Disease","country":"","productType":"Large molecule","year":"2024","type":"Not Applicable","leadProduct":"RCT2100","moa":"","graph1":"Genetic Disease","graph2":"Phase I","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"Ph I","therapeuticAreaShortName":"Genetic Disease","amount2New":0,"dosageForm":"Inhalation","sponsorNew":"ReCode Therapeutics \/ Not Applicable","highestDevelopmentStatusID":"6","companyTruncated":"ReCode Therapeutics \/ Not Applicable"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","therapeuticArea":"Rare Diseases and Disorders","country":"","productType":"Large molecule","year":"2024","type":"Not Applicable","leadProduct":"RCT1100","moa":"","graph1":"Rare Diseases and Disorders","graph2":"Phase I","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"Ph I","therapeuticAreaShortName":"Rare Diseases","amount2New":0,"dosageForm":"","sponsorNew":"ReCode Therapeutics \/ Not Applicable","highestDevelopmentStatusID":"6","companyTruncated":"ReCode Therapeutics \/ Not Applicable"},{"orgOrder":0,"company":"ReCode Therapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","therapeuticArea":"Genetic Disease","country":"","productType":"Large molecule","year":"2024","type":"Not Applicable","leadProduct":"RCT2100","moa":"","graph1":"Technology","graph2":"Phase I\/II","graph3":"ReCode Therapeutics","amount2":0,"highestDevelopmentShortName":"","therapeuticAreaShortName":"Technology","amount2New":0.94999999999999996,"dosageForm":"","sponsorNew":"ReCode Therapeutics \/ Not Applicable","highestDevelopmentStatusID":"14","companyTruncated":"ReCode Therapeutics \/ Not Applicable"}]

    Find Clinical Drug Pipeline Developments & Deals by ReCode Therapeutics

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                            01

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            Lead Product(s) : RCT2100

                            Therapeutic Area : Genetic Disease

                            Study Phase : Phase I/ Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            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.

                            Brand Name : RCT2100

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            September 26, 2024

                            Lead Product(s) : RCT2100

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Phase I/ Phase II

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            02

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            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.

                            Brand Name : RCT1100

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 27, 2024

                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            03

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            Lead Product(s) : RCT2100

                            Therapeutic Area : Genetic Disease

                            Study Phase : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            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.

                            Brand Name : RCT2100

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            February 21, 2024

                            Lead Product(s) : RCT2100

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            04

                            ReCode Therapeutics

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                            CPhI India 2024
                            Not Confirmed

                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : CRISPR-based Therapy

                            Therapeutic Area : Genetic Disease

                            Study Phase : Discovery Platform

                            Recipient : Intellia Therapeutics

                            Deal Size : Undisclosed

                            Deal Type : Collaboration

                            DEALS_DEV arrow-down

                            Intellia and ReCode Collaborate On Gene Editing Therapies for Cystic Fibrosis

                            Details : The collaboration combines Intellia’s CRISPR platform and ReCode’s selective Organ Targeting lipid nanoparticle to correct cystic fibrosis-causing gene mutations.

                            Brand Name : Undisclosed

                            Molecule Type : Cell and Gene therapy

                            Upfront Cash : Undisclosed

                            February 15, 2024

                            Lead Product(s) : CRISPR-based Therapy

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Discovery Platform

                            Recipient : Intellia Therapeutics

                            Deal Size : Undisclosed

                            Deal Type : Collaboration

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                            05

                            ReCode Therapeutics

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                            CPhI India 2024
                            Not Confirmed

                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            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.

                            Brand Name : RCT1100

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            January 03, 2024

                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            06

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            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

                            DEALS_DEV arrow-down

                            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.

                            Brand Name : RCT1100

                            Molecule Type : Large molecule

                            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

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                            07

                            ReCode Therapeutics

                            U.S.A arrow
                            CPhI India 2024
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                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            ReCode Therapeutics Announces First Participants Dosed in a Phase 1 Healthy Volunteer Clinical Trial of Novel ...

                            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.

                            Brand Name : RCT1100

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            March 15, 2023

                            Lead Product(s) : RCT1100

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : Phase I

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            08

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : mRNA-based Therapy

                            Therapeutic Area : Genetic Disease

                            Study Phase : Preclinical

                            Sponsor : The Cystic Fibrosis Foundation

                            Deal Size : $15.0 million

                            Deal Type : Funding

                            DEALS_DEV arrow-down

                            ReCode Therapeutics Announces Strategic Investment from the Cystic Fibrosis Foundation to Accelerate Developme...

                            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.

                            Brand Name : ARCT-032

                            Molecule Type : Large molecule

                            Upfront Cash : Undisclosed

                            January 10, 2023

                            Lead Product(s) : mRNA-based Therapy

                            Therapeutic Area : Genetic Disease

                            Highest Development Status : Preclinical

                            Sponsor : The Cystic Fibrosis Foundation

                            Deal Size : $15.0 million

                            Deal Type : Funding

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                            09

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : Undisclosed

                            Therapeutic Area : Technology

                            Study Phase : Discovery Platform

                            Recipient : AskBio

                            Deal Size : Undisclosed

                            Deal Type : Collaboration

                            DEALS_DEV arrow-down

                            AskBio Announces Strategic Collaboration with ReCode Therapeutics to Explore Single Vector Gene Editing Platfo...

                            Details : AskBio will combine its synthetic DNA and gene editing nucleases with ReCode's selective organ targeting LNP technology to potentially create an all-in-one solution that enables full gene insertion by delivering with precision both the gene editing tool ...

                            Brand Name : Undisclosed

                            Molecule Type : Cell and Gene therapy

                            Upfront Cash : Undisclosed

                            January 09, 2023

                            Lead Product(s) : Undisclosed

                            Therapeutic Area : Technology

                            Highest Development Status : Discovery Platform

                            Recipient : AskBio

                            Deal Size : Undisclosed

                            Deal Type : Collaboration

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                            10

                            ReCode Therapeutics

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                            CPhI India 2024
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                            ReCode Therapeutics

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                            CPhI India 2024
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                            Lead Product(s) : SORT LNP-based DNAI1 mRNA Therapeutic

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : Preclinical

                            Sponsor : Leaps by Bayer

                            Deal Size : $200.0 million

                            Deal Type : Series B Financing

                            DEALS_DEV arrow-down

                            ReCode Therapeutics to Expand Next-Generation Delivery Platform and Diversify Genetic Medicines Pipeline with ...

                            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...

                            Brand Name : Undisclosed

                            Molecule Type : Large molecule

                            Upfront Cash : Undisclosed

                            June 29, 2022

                            Lead Product(s) : SORT LNP-based DNAI1 mRNA Therapeutic

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : Preclinical

                            Sponsor : Leaps by Bayer

                            Deal Size : $200.0 million

                            Deal Type : Series B Financing

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                            Data Compilation
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                            Virtual Booth