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// ECONOMICTIMES
https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/japanese-pharma-takeda-launches-innovation-centre-eyes-to-onboard-ai-driven-talent/articleshow/117272460.cms
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// FIERCE PHARMA
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28 Dec 2024
// PRESS RELEASE
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16 Dec 2024
// FIERCE PHARMA
https://www.fiercepharma.com/marketing/takeda-casts-new-line-first-dtc-campaign-hyqvia-cidp
12 Dec 2024
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2024/12/13/2996584/0/en/HUTCHMED-to-Receive-Milestone-Payment-from-Takeda-following-1st-European-Reimbursement-for-FRUZAQLA-fruquintinib.html
12 Dec 2024
// BUSINESSWIRE
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4476
Submission : 1982-01-25
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-441 - Rev 03
Issue Date : 2022-07-29
Type : Chemical
Substance Number : 1442
Status : Valid
NDC Package Code : 11532-1450
Start Marketing Date : 1990-10-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION (3.75mg/mL)
Marketing Category : DRUG FOR FURTHER PRO...
Registrant Name : Korea Takeda Pharmaceutical Co., Ltd.
Registration Date : 2022-10-26
Registration Number : 20221026-210-J-1393
Manufacturer Name : Takeda Pharmaceutical Company Limited
Manufacturer Address : Hikari Plant: 4720, Takeda, Mitsui, Hikari, Yamaguchi 743-8502, Japan
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8243
Submission : 1989-10-11
Status : Inactive
Type : II
Certificate Number : R1-CEP 2007-246 - Rev 05
Issue Date : 2020-03-11
Type : Chemical
Substance Number : 2296
Status : Valid
NDC Package Code : 47234-0923
Start Marketing Date : 2013-08-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, FOR SOLUTION (40mg/10mL)
Marketing Category : DRUG FOR FURTHER PRO...
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Registration Number : 218MF10632
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 4-1-1
Initial Date of Registration : 2006-07-20
Latest Date of Registration :
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Registration Number : 219MF10064
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 4-1-1
Initial Date of Registration : 2007-03-05
Latest Date of Registration :
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9365
Submission : 1991-09-30
Status : Active
Type : II
NDC Package Code : 11532-1450
Start Marketing Date : 1990-10-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION (3.75mg/mL)
Marketing Category : DRUG FOR FURTHER PRO...
Registrant Name : Korea Takeda Pharmaceutical Co., Ltd.
Registration Date : 2022-10-26
Registration Number : 20221026-210-J-1393
Manufacturer Name : Takeda Pharmaceutical Company Limited
Manufacturer Address : Hikari Plant: 4720, Takeda, Mitsui, Hikari, Yamaguchi 743-8502, Japan
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10416
Submission : 1993-08-13
Status : Active
Type : II
NDC Package Code : 11532-1450
Start Marketing Date : 1990-10-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION (3.75mg/mL)
Marketing Category : DRUG FOR FURTHER PRO...
Registrant Name : Korea Takeda Pharmaceutical Co., Ltd.
Registration Date : 2022-10-26
Registration Number : 20221026-210-J-1393
Manufacturer Name : Takeda Pharmaceutical Company Limited
Manufacturer Address : Hikari Plant: 4720, Takeda, Mitsui, Hikari, Yamaguchi 743-8502, Japan
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11395
Submission : 1995-03-24
Status : Active
Type : II
NDC Package Code : 11532-1450
Start Marketing Date : 1990-10-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION (3.75mg/mL)
Marketing Category : DRUG FOR FURTHER PRO...
Registrant Name : Korea Takeda Pharmaceutical Co., Ltd.
Registration Date : 2022-10-26
Registration Number : 20221026-210-J-1393
Manufacturer Name : Takeda Pharmaceutical Company Limited
Manufacturer Address : Hikari Plant: 4720, Takeda, Mitsui, Hikari, Yamaguchi 743-8502, Japan
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Registration Number : 218MF10629
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 4-1-1
Initial Date of Registration : 2006-07-20
Latest Date of Registration :
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26940
Submission : 2013-04-11
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Certificate Number : R2-CEP 1995-021 - Rev 10
Issue Date : 2023-08-11
Type : Chemical
Substance Number : 248
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5609
Submission : 1984-10-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3414
Submission : 1979-01-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2859
Submission : 1977-02-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2318
Submission : 1974-08-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7071
Submission : 1987-07-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10416
Submission : 1993-08-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16755
Submission : 2003-08-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7021
Submission : 1987-06-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4616
Submission : 1982-07-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6315
Submission : 1986-03-10
Status : Inactive
Type : II
Details:
Takeda will obtain an exclusive license to further develop, manufacture and commercialize elritercept, an engineered ligand trap, worldwide outside of mainland China, Hong Kong and Macau.
Lead Product(s): Elritercept
Therapeutic Area: Oncology Brand Name: KER-050
Study Phase: Phase IIIProduct Type: Large molecule
Recipient: Keros Therapeutics
Deal Size: $1,300.0 million Upfront Cash: $200.0 million
Deal Type: Licensing Agreement December 03, 2024
Lead Product(s) : Elritercept
Therapeutic Area : Oncology
Highest Development Status : Phase III
Recipient : Keros Therapeutics
Deal Size : $1,300.0 million
Deal Type : Licensing Agreement
Keros Therapeutics Announces Global License Agreement with Takeda to Advance Elritercept
Details : Takeda will obtain an exclusive license to further develop, manufacture and commercialize elritercept, an engineered ligand trap, worldwide outside of mainland China, Hong Kong and Macau.
Brand Name : KER-050
Molecule Type : Large molecule
Upfront Cash : $200.0 million
December 03, 2024
Details:
The collaboration aims to develop Takeda’s proprietary induced pluripotent stem cell (iPSC) derived CAR-T cell platform (iCAR-T) and iPSC-derived CAR-NK platform (iCAR-NK).
Lead Product(s): iCAR-T Cell Therapy
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: Discovery PlatformProduct Type: Cell and Gene therapy
Recipient: Alloy Therapeutics
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Collaboration November 20, 2024
Lead Product(s) : iCAR-T Cell Therapy
Therapeutic Area : Oncology
Highest Development Status : Discovery Platform
Recipient : Alloy Therapeutics
Deal Size : Undisclosed
Deal Type : Collaboration
Alloy Therapeutics Partners with Takeda On iPSC-Derived Cell Therapies
Details : The collaboration aims to develop Takeda’s proprietary induced pluripotent stem cell (iPSC) derived CAR-T cell platform (iCAR-T) and iPSC-derived CAR-NK platform (iCAR-NK).
Brand Name : Undisclosed
Molecule Type : Cell and Gene therapy
Upfront Cash : Undisclosed
November 20, 2024
Details:
Takeda has the exclusive worldwide license to further develop, commercialize, and manufacture fruquintinib outside of mainland China, Hong Kong and Macau, and markets under the Fruzaqla brand name.
Lead Product(s): Fruquintinib
Therapeutic Area: Oncology Brand Name: Fruzaqla
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Hutchmed
Deal Size: $1,130.0 million Upfront Cash: $400.0 million
Deal Type: Licensing Agreement October 31, 2024
Lead Product(s) : Fruquintinib
Therapeutic Area : Oncology
Highest Development Status : Approved
Recipient : Hutchmed
Deal Size : $1,130.0 million
Deal Type : Licensing Agreement
HUTCHMED to Receive First Commercial Milestone Payment for Fruzaqla Sales by Takeda
Details : Takeda has the exclusive worldwide license to further develop, commercialize, and manufacture fruquintinib outside of mainland China, Hong Kong and Macau, and markets under the Fruzaqla brand name.
Brand Name : Fruzaqla
Molecule Type : Small molecule
Upfront Cash : $400.0 million
October 31, 2024
Details:
Takeda has elected to terminate its option to continue work on Wave’s WVE-003, a first-in-class, allele-selective antisense oligonucleotide, clinical-stage Huntington’s disease program.
Lead Product(s): WVE-003
Therapeutic Area: Genetic Disease Brand Name: WVE-003
Study Phase: Phase I/ Phase IIProduct Type: Large molecule
Recipient: Wave Life Sciences
Deal Size: $260.0 million Upfront Cash: $170.0 million
Deal Type: Termination October 16, 2024
Lead Product(s) : WVE-003
Therapeutic Area : Genetic Disease
Highest Development Status : Phase I/ Phase II
Recipient : Wave Life Sciences
Deal Size : $260.0 million
Deal Type : Termination
Takeda Walks Away from Wave Huntington’s Partnership After Sinking $260M in Collaboration
Details : Takeda has elected to terminate its option to continue work on Wave’s WVE-003, a first-in-class, allele-selective antisense oligonucleotide, clinical-stage Huntington’s disease program.
Brand Name : WVE-003
Molecule Type : Large molecule
Upfront Cash : $170.0 million
October 16, 2024
Details:
The collaboration seeks to leverage Tempus' multimodal real-world datasets and biological modeling capabilities to enhance Takeda’s pipeline of cancer therapeutics.
Lead Product(s): Undisclosed
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: UndisclosedProduct Type: Large molecule
Recipient: Tempus
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Collaboration September 26, 2024
Lead Product(s) : Undisclosed
Therapeutic Area : Oncology
Highest Development Status : Undisclosed
Recipient : Tempus
Deal Size : Undisclosed
Deal Type : Collaboration
Tempus Expands Collaboration with Takeda for Multimodal Oncology Research
Details : The collaboration seeks to leverage Tempus' multimodal real-world datasets and biological modeling capabilities to enhance Takeda’s pipeline of cancer therapeutics.
Brand Name : Undisclosed
Molecule Type : Large molecule
Upfront Cash : Undisclosed
September 26, 2024
Details:
Fruzaqla (fruquintinib) is the first and only selective inhibitor of all three VEGF receptor kinases approved for previously treated mCRC regardless of biomarker status.
Lead Product(s): Fruquintinib
Therapeutic Area: Oncology Brand Name: Fruzaqla
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 24, 2024
Lead Product(s) : Fruquintinib
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Takeda Receives Approval for FRUZAQLA in Japan for Advanced Colorectal Cancer
Details : Fruzaqla (fruquintinib) is the first and only selective inhibitor of all three VEGF receptor kinases approved for previously treated mCRC regardless of biomarker status.
Brand Name : Fruzaqla
Molecule Type : Small molecule
Upfront Cash : Not Applicable
September 24, 2024
Details:
Under the terms of this agreement, Takeda has granted Lupin non-exclusive patent licensing rights to commercialize Lupivon (vonoprazan), a novel potassium-competitive acid blocker, in India.
Lead Product(s): Vonoprazan Fumarate
Therapeutic Area: Gastroenterology Brand Name: Lupivon
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Lupin Ltd
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement September 18, 2024
Lead Product(s) : Vonoprazan Fumarate
Therapeutic Area : Gastroenterology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Lupin Ltd
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Lupin Partners with Takeda to Commercialise Vonoprazan
Details : Under the terms of this agreement, Takeda has granted Lupin non-exclusive patent licensing rights to commercialize Lupivon (vonoprazan), a novel potassium-competitive acid blocker, in India.
Brand Name : Lupivon
Molecule Type : Small molecule
Upfront Cash : Undisclosed
September 18, 2024
Details:
The licensing deal will enhance Alkem's offerings in the gastrointestinal segment by including Vonzai (vonoprazan), a first-in-class potassium-competitive acid blocker.
Lead Product(s): Vonoprazan Fumarate
Therapeutic Area: Gastroenterology Brand Name: Vonzai
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Alkem Laboratories
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement September 03, 2024
Lead Product(s) : Vonoprazan Fumarate
Therapeutic Area : Gastroenterology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Alkem Laboratories
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Alkem Inks Licensing Pact with Takeda to Introduce Vonoprazan in India
Details : The licensing deal will enhance Alkem's offerings in the gastrointestinal segment by including Vonzai (vonoprazan), a first-in-class potassium-competitive acid blocker.
Brand Name : Vonzai
Molecule Type : Small molecule
Upfront Cash : Undisclosed
September 03, 2024
Details:
The collaboartion aims to develop innovative novel plasma-derived therapy formulations for the treatment of rare conditions. Nanoform will provide non-GMP nanomaterial to Takeda for in vivo studies.
Lead Product(s): Plasma-derived Therapy
Therapeutic Area: Rare Diseases and Disorders Brand Name: Undisclosed
Study Phase: PreclinicalProduct Type: Large molecule
Recipient: Nanoform
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Collaboration August 15, 2024
Lead Product(s) : Plasma-derived Therapy
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Preclinical
Recipient : Nanoform
Deal Size : Undisclosed
Deal Type : Collaboration
Nanoform Collaborates with Takeda on their Plasma-derived Therapy Development
Details : The collaboartion aims to develop innovative novel plasma-derived therapy formulations for the treatment of rare conditions. Nanoform will provide non-GMP nanomaterial to Takeda for in vivo studies.
Brand Name : Undisclosed
Molecule Type : Large molecule
Upfront Cash : Undisclosed
August 15, 2024
Details:
Adzynma (apadamtase alfa /cinaxadamtase alfa) is the first and only ADAMTS13 enzyme replacement therapy, which is approved for the treatment of congenital thrombotic thrombocytopenic purpura.
Lead Product(s): Apadamtase Alfa,Cinaxadamtase Alfa
Therapeutic Area: Rare Diseases and Disorders Brand Name: Adzynma
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable August 08, 2024
Lead Product(s) : Apadamtase Alfa,Cinaxadamtase Alfa
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Takeda Receives EU Approval for ADZYNMA® as First ADAMTS13 Replacement in cTTP
Details : Adzynma (apadamtase alfa /cinaxadamtase alfa) is the first and only ADAMTS13 enzyme replacement therapy, which is approved for the treatment of congenital thrombotic thrombocytopenic purpura.
Brand Name : Adzynma
Molecule Type : Large molecule
Upfront Cash : Not Applicable
August 08, 2024
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Brand Name : Adrenalin
Dosage Strength : 0.1mg/ml
Packaging : Ampoule av glass 10 5ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Brand Name : Adrenalin
Dosage Strength : 1mg/ml
Packaging : Ampoule av glass 10 1ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : JEL
Brand Name : Reparil Gel
Dosage Strength : 1g/100g
Packaging : 40X1g/100g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : JEL
Brand Name : Reparil Gel
Dosage Strength : 1g/100g
Packaging : 20X1g/100g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : JEL
Brand Name : Reparil Gel
Dosage Strength : 1g/100g
Packaging : 100X1g/100g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : REPLAGAL
Dosage Strength : 1MG/ML
Packaging :
Approval Date :
Application Number : 2249057
Regulatory Info :
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INF
Brand Name : Replagal
Dosage Strength : 1mg/ml
Packaging : 3.5X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Conc
Brand Name : Replagal
Dosage Strength : 3.5mg/3.5ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet
Brand Name : Allopur
Dosage Strength : 300 mg
Packaging : Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Sweden
Dosage Form : TABLET
Brand Name : Allopurinol Nycomed
Dosage Strength : 100 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 0.1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Switzerland
Dosage Form : Inf Conc
Dosage Strength : 3.5mg/3.5ml
Packaging :
Brand Name : Replagal
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Sweden
Dosage Form : TABLET
Dosage Strength : 300 MG
Packaging :
Brand Name : Allopurinol Nycomed
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Dosage Form : TABLET
Dosage Strength : 100 MG
Packaging :
Brand Name : Allopurinol Nycomed
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet
Dosage Strength : 100 mg
Packaging : Box
Brand Name : Allopur
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet
Dosage Strength : 300 mg
Packaging : Box
Brand Name : Allopur
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 12.5 mg
Packaging : Blister
Brand Name : Vipidia
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 12.5 mg
Packaging : Blister
Brand Name : Vipidia
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 25 mg
Packaging : Blister
Brand Name : Vipidia
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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TAKEDA is a supplier offers 30 products (APIs, Excipients or Intermediates).
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