SBIR-STTR Award

PDE4D Pet Ligand
Award last edited on: 2/2/2021

Sponsored Program
SBIR
Awarding Agency
NIH : NIMH
Total Award Amount
$1,923,913
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Mark E Gurney

Company Information

Tetra Discovery Partners LLC

301 Michigan Street Ne Suite 531
Grand Rapids, MI 49503
   (616) 635-0937
   mark@tetradiscovery.com
   www.tetradiscovery.com
Location: Multiple
Congr. District: 03
County: Kent

Phase I

Contract Number: 1R43MH107077-01
Start Date: 7/1/2015    Completed: 6/30/2016
Phase I year
2015
Phase I Amount
$346,237
Tetra Discovery Partners is the recipient of an NIH Blueprint Neurotherapeutics Network award to develop phosphodiesterase-4D (PDE4D) Negative Allosteric Modulators (NAMs) for treating memory loss in patients affected by psychiatric and neurologic diseases. The Tetra-NIH Blueprint drug is projected to reach human Phase I clinical trials in late 2015. Through a Cooperative Research and Development Agreement (CRADA) with Dr Robert Innis and Dr Victor Pike of the NIMH Intramural Program, the company has been working in parallel to develop novel PET ligands for imaging PDE4 subtypes in the human brain. The goal of the proposed Phase I SBIR is to develop a PDE4D PET ligand useful for assessing target occupancy in human Phase I clinical trials of the Tetra-NIH Blueprint drug as well as a PET ligand that will be useful for assessing PDE4D levels in patients with psychiatric and neurologic disease. PDE4D as a target for improving cognition in humans has genetic validation through studies of children with PDE4D gene mutations who develop an ultra-rare disorder known as acrodysostosis type-2 (ACRDY2; MIM 600129). ACRDY2 is a developmental disorder characterized by intellectual disability, brachydactyly, nasal hypoplasia and short stature. Children with acrodysostosis only achieve an IQ of 50-80. Thus, PDE4D is the human ortholog of the Drosophila PDE4 gene in which the Dunce mutation was the first learning mutation identified in a model organism. Rolipram and other PDE4 inhibitors have been shown to be broadly pro-cognitive in numerous animal models of learning and memory, while knock-out or knock-down of the mouse PDE4D gene also improves learning and memory. Our NIMH collaborators, Innis and Pike, have shown that PDE4 PET imaging is altered in patients with major depression. Those studies used C-11 (R)-rolipram as a PET ligand for assessing PDE4 levels, however, rolipram binds equally to the different subtypes of PDE4 expressed in brain (PDE4A, PDE4B & PDE4D). We therefore want to understand if PDE4D levels are altered in major depression and other psychiatric diseases. In the Phase I SBIR, Tetra will optimize potent and selective PDE4D NAMs for C-11 or F-18 labelling by Innis and Pike who will conduct in vivo PET imaging studies. Should a suitable PDE4D PET ligand be identified, the imaging agent could rapidly advance into human clinical trials.

Public Health Relevance Statement:


Public Health Relevance:
The company has developed a mechanistically novel class of drugs to address cognitive impairment across multiple psychiatric and neurological indications. These new drugs are Negative Allosteric Modulators (NAMs) of phosphodiesterase-4D (PDE4D). The SBIR project will develop a PDE4D selective PET ligand to be used in human Phase I clinical trials of the cognition drug to assess PDE4D target occupancy.

Project Terms:
Acrodysostosis; Active Sites; Address; Affect; Amino Acids; Animal Model; Award; Binding (Molecular Function); Binding Sites; Brain; Child; Clinical Trials; Cognition; Cognitive; Cooperative Research and Development Agreement; Databases; design; developmental disease/disorder; Disease; Drosophila genus; Enzymes; Funding; G Protein-Coupled Receptor Genes; Gene Mutation; Genes; Genetic; genotoxicity; Goals; Health; Human; Image; Impaired cognition; improved; in vivo; inhibitor/antagonist; Inhibitory Concentration 50; Intellectual functioning disability; Intramural Research Program; Ion Channel; knock-down; Knock-out; Label; Lead; Learning; Ligands; Major Depressive Disorder; Memory; Memory Loss; Mental disorders; Metabolic Activation; Monkeys; Mus; Mutation; National Institute of Mental Health (U.S.); Neurologic; Nose; novel; Orthologous Gene; Patients; PDE4B; Pharmaceutical Chemistry; Pharmaceutical Preparations; Phase; Phase I Clinical Trials; Phenylalanine; phosphodiesterase 4D; Pike fish; Plasma; Plasma Proteins; Positron-Emission Tomography; Protein Binding; Rare Diseases; Rattus; Rolipram; Small Business Innovation Research Grant; Structure; Testing; Tyrosine; United States National Institutes of Health; Validation; Work

Phase II

Contract Number: 2R44MH107077-02A1
Start Date: 7/1/2015    Completed: 4/30/2019
Phase II year
2018
(last award dollars: 2020)
Phase II Amount
$1,577,676

Tetra Discovery Partners is submitting a Phase II SBIR application to develop a phosphodiesterase-4D (PDE4D) PET tracer for imaging the distribution of the enzyme in human brain. Tetra is a clinical stage biotechnology company that is developing BPN14770, a PDE4D negative allosteric modulator (PDE4D-NAM), as a treatment for cognitive impairment in Alzheimer’s disease, other dementias and psychiatric disorders including schizophrenia and major depressive disorder (MDD). Human studies with the PDE4D PET tracer may benefit patients by improving understanding of how changes in cAMP signaling and altered regulation of PDE4 subtypes contribute to the pathophysiology of disease. The PET tracer will be useful for determining the dose of BPN14770 to be used in pivotal human clinical trials by assessing PDE4D target occupancy in brain. The target occupancy study adds value to the BPN14770 neurotherapeutic and is a critical gate keeper for partnering the drug program with a larger pharmaceutical company. Tetra has completed a successful Phase I SBIR in which a lead PET tracer has been developed that shows specific, displaceable binding to PDE4D in rhesus monkey brain. PET imaging was performed in monkeys as only primate PDE4D contains a key phenylalanine residue on the UCR2 regulatory domain required for PDE4D subtype selectivity. The PET imaging study revealed an intriguing pattern of specific PDE4D binding in regions of the brain known to be important for cognition, namely prefrontal cortex, temporal cortex and hippocampus. However, accumulation of radiolabeled metabolites precludes further advancement of the compound. The Phase II SBIR proposes a straightforward chemical optimization strategy to address this issue. The goal of the Phase II SBIR is to optimize a PDE4D PET ligand for advancement into human clinical trials.

Public Health Relevance Statement:
The SBIR project will develop a PDE4D selective PET imaging agent to be used in human clinical trials. Human studies with the PDE4D PET tracer may benefit patients with major depressive disorder by improving understanding of the disease. The PDE4D PET tracer will also guide BPN14770 dose selection for pivotal human clinical trials. BPN14770 is a mechanistically novel drug targeting PDE4D that is being developed by Tetra to address disorders of learning and memory across multiple psychiatric and neurological indications.

Project Terms:
Address; Alzheimer's Disease; base; Binding; Biotechnology; Brain; Brain region; Chemicals; Clinical; Clinical Trials; Cognition; Collaborations; Cooperative Research and Development Agreement; Cyclic AMP; Dementia; Disease; Dose; Elderly; Enzymes; Functional disorder; G-Protein-Coupled Receptors; Goals; Hippocampus (Brain); Human; Image; imaging agent; imaging study; Impaired cognition; improved; In Vitro; inhibitor/antagonist; Intramural Research Program; Investigational New Drug Application; Ion Channel; Label; Lead; Learning Disorders; Libraries; Ligands; Macaca fascicularis; Macaca mulatta; Major Depressive Disorder; Memory; Mental disorders; Methods; Modeling; Monkeys; Mus; National Institute of Mental Health; Neurologic; new therapeutic target; Noise; Patients; Pattern; Pharmaceutical Preparations; Pharmacologic Substance; Phase; Phenylalanine; phosphodiesterase 4D; Pike fish; Plasma; Positron-Emission Tomography; pre-clinical; Prefrontal Cortex; Primates; programs; Radiolabeled; Radiology Specialty; Rattus; Regulation; Schizophrenia; Signal Transduction; Small Business Innovation Research Grant; Temporal Lobe; Toxic effect; Toxicology; Tracer; uptake