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  • CREAM;TOPICAL - 2.5%;2.5%
  • PATCH;TOPICAL - 5%
  • PATCH;TOPICAL - 70MG;70MG
  • CREAM;TOPICAL - 7%;7%

Details:

JUVÉDERM® VOLBELLA® XC was first FDA–approved in 2016 for use in the lips and perioral rhytids.2 As the category leader, the JUVÉDERM® Collection of Fillers offers the broadest portfolio, and this latest approval marks the sixth approved indication in the U.S.


Lead Product(s): Hyaluronic Acid,Lidocaine

Therapeutic Area: Dermatology Product Name: Juvéderm Volbella XC

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 08, 2022

Abbvie CB

Iran Expo

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envelop Contact Supplier

Details:

The net proceeds will be used for the commercialisation of ZTlido® (lidocaine topical system), a prescription lidocaine topical product approved by the FDA for the relief of neuropathic pain associated with postherpetic neuralgia, which is a form of post-shingles nerve pain.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: Ztlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Rodman & Renshaw LLC

Deal Size: $10.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering March 05, 2024

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The net proceeds will be used for the commercialisation of ZTlido® (lidocaine topical system), a prescription lidocaine topical product approved by the FDA for the relief of neuropathic pain associated with postherpetic neuralgia, which is a form of post-shingles nerve pain.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: Ztlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Rodman & Renshaw LLC

Deal Size: $10.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering February 29, 2024

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SP-103 (lidocaine topical system) 5.4% triple strength formulation for ZTlido®, is being investigated in subjects with moderate to severe acute lower back pain (LBP).


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: SP-103

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 14, 2023

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Details:

Alenura is a unique, combination product of alkalinised lidocaine and the glycosaminoglycan heparin. Alkalinised lidocaine penetrates the transitional epithelial cell layer and provides immediate pain relief.


Lead Product(s): Lidocaine,Heparin Sodium

Therapeutic Area: Urology Product Name: Alenura

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Vaneltix Pharma

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 22, 2023

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CITI-002 (lidocaine-halobetasol propionate) is a proprietary topical formulation intended to provide symptomatic relief to individuals suffering from hemorrhoids, a gastrointestinal disorder characterized by pain, swelling, itching, tenderness, and bleeding.


Lead Product(s): Lidocaine,Halobetasol

Therapeutic Area: Gastroenterology Product Name: CITI-002

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 20, 2023

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Princess Volume Plus (hyaluronic acid) dermal filler and Lidocaine with the intention to confirm the efficacy and safety in respect of mid-facial volume insufficiency and/or mid-facial profile deficient participants.


Lead Product(s): Hyaluronic Acid,Lidocaine

Therapeutic Area: Dermatology Product Name: Princess Volume Plus

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 June 12, 2023

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The agreement aims for the distribution of Ztlido (lidocaine), a lidocaine topical system approved for the relief of neuropathic pain associated with post-herpetic neuralgia, in Kingdom of Saudi Arabia.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: Ztlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Farouk, Maamoun Tamer & Co.

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement May 31, 2023

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SP-103 (lidocaine topical system) 5.4% triple strength formulation for ZTlido®, is being investigated in subjects with moderate to severe acute lower back pain (LBP).


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: SP-103

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 04, 2023

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Details:

CITI-002 (lidocaine-halobetasol propionate) is a proprietary topical formulation intended to provide symptomatic relief to individuals suffering from hemorrhoids, a gastrointestinal disorder characterized by pain, swelling, itching, tenderness, and bleeding.


Lead Product(s): Lidocaine,Halobetasol

Therapeutic Area: Gastroenterology Product Name: CITI-002

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 03, 2023

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Details:

Proceeds from the financing commitment will be used to enhance the launch and commercialization of Scilex’s three FDA-approved non-opioid pain management products, ZTlido (lidocaine), Gloperba (colchicine) and Elyxyb (celecoxib), for the treatment of acute and chronic pain.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: Ztlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: YA II PN

Deal Size: $25.0 million Upfront Cash: Undisclosed

Deal Type: Financing March 21, 2023

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Details:

SP-103 has three times the drug load of ZTlido® (Lidocaine - 108 mg versus 36 mg) in the same adhesive system to potentially deliver a three-fold level of the drug within a targeted area, but retaining the convenience of a single topical system.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: SP-103

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 30, 2022

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Details:

ZTlido® (lidocaine topical system) 1.8%, or ZTlido®, is a prescription lidocaine topical product approved by the U.S. Food and Drug Administration for the relief of pain associated with postherpetic neuralgia, which is a form of post-shingles nerve pain.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: ZTlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: CH Trading Group

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement August 17, 2022

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ZTlido® (lidocaine topical system) 1.8%, a best-in-class prescription lidocaine topical product used for relief of pain from damaged nerves (neuropathic pain) that follows healing of shingles.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: ZTlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 02, 2022

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Details:

Halo-Lido is a proprietary topical formulation of halobetasol and lidocaine that is intended to provide symptomatic relief to individuals suffering from hemorrhoids, a gastrointestinal disorder.


Lead Product(s): Halobetasol,Lidocaine

Therapeutic Area: Gastroenterology Product Name: Halo-Lido

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 26, 2022

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Details:

Under the terms of the agreement, Vaneltix will be responsible for the further development, manufacturing, regulatory affairs and commercialisation of AlenuraTM in collaboration with Hyloris.


Lead Product(s): Lidocaine,Heparin Sodium

Therapeutic Area: Urology Product Name: Alenura

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Hyloris Pharmaceuticals

Deal Size: $6.7 million Upfront Cash: Undisclosed

Deal Type: Collaboration December 17, 2021

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Details:

The formulation contains a eutectic mixture of 7% lidocaine and 7% tetracaine that utilizes phase-changing topical cream Peel technology. In clinical studies, the mean duration of anesthesia has been shown to be in the range of 7 to 9 hours after the application of Pliaglis.


Lead Product(s): Lidocaine,Tetracaine

Therapeutic Area: Neurology Product Name: Pliaglis

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Egis Pharmaceuticals PLC

Deal Size: Undisclosed Upfront Cash: $0.7 million

Deal Type: Licensing Agreement December 13, 2021

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Details:

Scilex is dedicated to the development and commercialization of non-opioid pain management products for treatment of acute and chronic pain. Scilex’s product ZTLIDO ® (lidocaine topical system) 1.8%, a non-opioid prescription lidocaine topical product approved by the U.S. FDA.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: Ztlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Vickers Vantage Corp I

Deal Size: $1,640.0 million Upfront Cash: Undisclosed

Deal Type: Agreement December 06, 2021

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Details:

Under the terms of the Agreement, STADA will be responsible for commercializing Pliaglis in the Territories utilizing its experienced sales force.


Lead Product(s): Lidocaine,Tetracaine

Therapeutic Area: Neurology Product Name: Pliaglis

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: STADA Arzneimittel

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement August 18, 2021

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The in-vitro and animal data suggest that TRG-100 can safely be used for possible intravesical sustained release of Lidocaine and Oxybutynin in the treatment of BPS/IC.


Lead Product(s): Oxybutynin,Lidocaine

Therapeutic Area: Urology Product Name: TRG-100

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 22, 2021

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Details:

Croma will promote Pliaglis directly to physicians through its sales network consisting of approximately 130 members across the Territories. As part of the agreement, Crescita is eligible to receive a combination of upfront, cumulative sales and other milestone payments.


Lead Product(s): Lidocaine,Tetracaine

Therapeutic Area: Neurology Product Name: Pliaglis

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Croma-Pharma

Deal Size: $1.4 million Upfront Cash: Undisclosed

Deal Type: Licensing Agreement June 28, 2021

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Details:

ZTlido® is the only lidocaine topical system that has been studied under the water stress conditions, and now has FDA label reflecting its use while showering, swimming and bathing.


Lead Product(s): Lidocaine

Therapeutic Area: Neurology Product Name: ZTlido

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 09, 2021

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Details:

Restylane Defyne is a hyaluronic acid (HA) dermal filler that was first approved in 2016 by the FDA for mid-to-deep injection into the facial tissue for the correction of moderate to severe deep facial wrinkles and folds, such as nasolabial folds, in patients over age 21.


Lead Product(s): Hyaluronic Acid,Lidocaine

Therapeutic Area: Dermatology Product Name: Restylane Defyne

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 01, 2021

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Under the License Agreement Regent Pacific is now entitled to receive a payment of approximately HK$6.24 million from Wanbang Pharmaceutical, which is payable within 30 business days. NMPA will now formally review Senstend™ for Clinical Trial Approval.


Lead Product(s): Lidocaine,Prilocaine

Therapeutic Area: Psychiatry/Psychology Product Name: Senstend

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Wanbang Biopharmaceuticals

Deal Size: $4.0 million Upfront Cash: Undisclosed

Deal Type: Licensing Agreement December 02, 2020

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Details:

Under the terms of the agreement, Juyou will look after overall clinical development and regulatory filings for Pliaglis with the National Medical Products Administration (the "NMPA", formerly the China State Food and Drug Administration.


Lead Product(s): Lidocaine,Tetracaine

Therapeutic Area: Neurology Product Name: Pliaglis

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Juyou Biotechnology

Deal Size: $2.9 million Upfront Cash: $0.1 million

Deal Type: Licensing Agreement November 05, 2020

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Company’s field force is established and will begin introducing its prestige aesthetics portfolio, including the RHA® Collection of dermal fillers, resilient hyaluronic acid, and the HintMD financial technology (fintech) platform, in the United States (U.S.) in September.


Lead Product(s): Hyaluronic Acid,Lidocaine

Therapeutic Area: Dermatology Product Name: RHA

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 25, 2020

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Details:

The Company continues to pursue out-licensing partnerships with focus on approximately 20 countries where Pliaglis has already received regulatory approval.


Lead Product(s): Lidocaine,Tetracaine

Therapeutic Area: Neurology Product Name: Pliaglis

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Taro Pharmaceutical Industries

Deal Size: Undisclosed Upfront Cash: $3.9 million

Deal Type: Licensing Agreement July 28, 2020

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The partnership with FILLMED will allow Crescita to expand its product offering in the medical aesthetic field with the addition of the hyaluronic acid ART-Filler® injectables range and NCTF® 135 HA.


Lead Product(s): Lidocaine,Hyaluronic Acid

Therapeutic Area: Dermatology Product Name: Undisclosed

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Crescita Therapeutics

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement January 20, 2020

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Under the agreement Revance will gain immediate and exclusive rights to commercialize TEOXANE’s RHA® line of fillers in the U.S.


Lead Product(s): Hyaluronic Acid,Lidocaine

Therapeutic Area: Musculoskeletal Product Name: Undisclosed

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Revance Therapeutics

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement January 09, 2020

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