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Grunenthal
Germany Flag
Country
Country
Germany
Address
Address
Zieglerstraße 6, 52078 Aachen
Telephone
Telephone
+ 49 241 569 3231

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Details:

The joint venture collaboration comprises 13 brands across 6 therapeutic areas primarily focused on pain management, including Abstral (fentanyl) and PecFent for breakthrough cancer pain, Moventig for opioid-induced constipation, and Adcal-D3® for osteoporosis.


Lead Product(s): Fentanyl

Therapeutic Area: Neurology Product Name: Abstral

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Grunenthal Meds

Deal Size: $83.2 million Upfront Cash: Undisclosed

Deal Type: Collaboration August 02, 2023

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The collaboration leads to the successful reformulation of an investigational, orally dosed small molecule in Grünenthal’s pipeline to improve its bioavailability. Phase 1 studies of the molecule will be supported by using the Catalent Xpress Pharmaceutics™ platform.


Lead Product(s): Undisclosed

Therapeutic Area: Neurology Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Small molecule

Recipient: Catalent Pharma Solutions

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration March 15, 2023

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Key products in the portfolio include Abstral® and PecFent® (Fentanyl) for breakthrough cancer pain, Moventig® (Naloxegol) for opioid-induced constipation and Adcal-D3® (calcium and vitamin D3) for osteoporosis.


Lead Product(s): Fentanyl

Therapeutic Area: Neurology Product Name: Abstral

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Kyowa Kirin

Deal Size: Undisclosed Upfront Cash: $82.7 million

Deal Type: Collaboration November 24, 2022

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Nebido (having testosterone undecanoate) is the only available injectable long-acting depot preparation of testosterone undecanoate, developed for the treatment of male hypogonadism.


Lead Product(s): Testosterone Undecanoate

Therapeutic Area: Endocrinology Product Name: Nebido

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Bayer AG

Deal Size: $498.1 million Upfront Cash: Undisclosed

Deal Type: Acquisition November 02, 2022

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Details:

RTX is an intra-articular injection of resiniferatoxin developed for the treatment of pain in patients with moderate to severe pain associated with knee osteoarthritis.


Lead Product(s): Resiniferatoxin

Therapeutic Area: Rheumatology Product Name: RTX

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 18, 2022

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The agreement includes competitive investment commitments for launch and commercialisation. Manufacturing and supply of RTX (resiniferatoxin) to Shionogi will be carried out exclusively by Grünenthal.


Lead Product(s): Resiniferatoxin

Therapeutic Area: Rheumatology Product Name: RTX

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Shionogi

Deal Size: $670.0 million Upfront Cash: Undisclosed

Deal Type: Licensing Agreement August 04, 2022

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Nebido (testosterone undecanoate) is used for male hypogonadism. It is used for treating clinical symptoms such as regression of secondary sexual characteristics, change in body composition, asthenia, reduced libido or erectile dysfunction due to low testosterone levels.


Lead Product(s): Testosterone Undecanoate

Therapeutic Area: Endocrinology Product Name: Nebido

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Bayer AG

Deal Size: $506.6 million Upfront Cash: Undisclosed

Deal Type: Acquisition July 14, 2022

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A key objective of MPC-06-ID (rexlemestrocel-L) is to demonstrate reduction in pain and opioid usage and and position rexlemestrocel-L as a potential opioid-sparing agent.


Lead Product(s): Rexlemestrocel-L,Hyaluronic Acid

Therapeutic Area: Neurology Product Name: MPC-06-ID

Highest Development Status: Phase IIIProduct Type: Cell and Gene therapy

Recipient: Mesoblast

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 15, 2021

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Details:

The Phase III study investigates the efficacy, safety, and tolerability of QUTENZA (capsaicin) 8% topical system in post-surgical neuropathic pain (PSNP) to support an extension of the U.S. label.


Lead Product(s): Capsaicin

Therapeutic Area: Neurology Product Name: Qutenza

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 10, 2021

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Phase III studies investigating efficacy, safety and tolerability of Qutenza (capsaicin) 8% topical system in post-surgical neuropathic pain (PSNP) and the efficacy, safety and tolerability of Resiniferatoxin in patients with pain associated with osteoarthritis of the knee.


Lead Product(s): Undisclosed

Therapeutic Area: Immunology Product Name: Undisclosed

Highest Development Status: Phase IProduct Type: Undisclosed

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 27, 2021

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