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Idera Pharmaceuticals
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Country
U.S.A
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Address
Pennsylvania 505 Eagleview Boulevard Suite 212 Exton, PA 19341
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Telephone
484-348-1600

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The combined cash of the two companies is expected to provide runway into Q3 2023, funding the advancement of Aceragen’s pipeline, including ACG-701 (sodium fusidate) and ACG-801, through important 2023 clinical milestones.


Lead Product(s): Sodium Fusidate,Ceftazidime,Meropenem

Therapeutic Area: Infections and Infectious Diseases Product Name: ACG-701

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Recipient: Aceragen

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Acquisition September 28, 2022

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Tilsotolimod is an investigational, synthetic Toll-like receptor 9 agonist. Tilsotolimod (IMO-2125) has been shown to promote both innate (Type-I IFN, antigen presentation) and adaptive immune activation and may, in turn, contribute to tumor suppression and regression.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 17, 2022

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Company announced clinical updates regarding IMO-2125 (tilsotolimod), its synthetic Toll-like receptor 9 agonist has been shown to promote both innate (Type-I IFN, antigen presentation) and adaptive (T cells) immune activation.


Lead Product(s): Tilsotolimod,Nivolumab,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: Phase II/ Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: AbbVie Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 14, 2021

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ILLUMINATE-301 is a randomized, global, multi-center, open label Phase 3 trial comparing the efficacy of 8 mg intratumoral tilsotolimod in combination with 3 mg/kg ipilimumab versus 3 mg/kg ipilimumab alone in 481 patients with anti-PD-1 refractory advanced melanoma.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Bristol Myers Squibb

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 18, 2021

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The Company plans to use the $10.0 million in cash proceeds to fund the completion of the ongoing ILLUMINATE-301 clinical trial and potential NDA filing of its lead product, tilsotolimod, for the treatment of anti-PD-1 refractory metastatic melanoma.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Undisclosed

Deal Size: $20.7 million Upfront Cash: Undisclosed

Deal Type: Private Placement December 15, 2020

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This new coverage expands protection of the first tilsotolimod method-of-use patent, which was directed to methods of treating metastatic melanoma and was issued in November 2019.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 28, 2020

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ILLUMINATE-204 is a multi-center, two-arm phase 1/2 trial in patients with anti-PD-1 refractory advanced melanoma. The phase 1 portion of the trial tested the safety and efficacy of increasing doses of tilsotolimod in combination with either Yervoy®* or Keytruda®.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 15, 2020

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The Company plans to use the initial proceeds and, if exercised, subsequent proceeds from the financing for the ongoing clinical development of tilsotolimod, its potential NDA filing and commercial launch, and for general corporate purposes.


Lead Product(s): Tilsotolimod,Ipilimumab

Therapeutic Area: Oncology Product Name: IMO-2125

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Undisclosed

Deal Size: $20.0 million Upfront Cash: Undisclosed

Deal Type: Private Placement July 15, 2020

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Tilsotolimod in combination with Opdivo® (nivolumab) and Yervoy®* (ipilimumab) was generally well tolerated; no patients discontinued treatment due to adverse events (AEs) and none experienced Grade 4 or 5 AEs.


Lead Product(s): Tilsotolimod,Ipilimumab,Nivolumab

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: Phase II/ Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 02, 2020

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The combination regimen was generally well tolerated among the 62 patients receiving tilsotolimod at any dose in combination with Yervoy® in the ILLUMINATE-204 clinical trial.


Lead Product(s): Tilsotolimod,Ipilimumab,Pembrolizumab

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 21, 2020

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