New drug approvals - November 2021

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Product Name

SLINDA FILM-COATED TABLETS 4MG

Active Ingredient

Drospirenone

Application type

NDA-2

Product Registrant

Intega Pte Ltd

Date of Approval

01/11/2021

Registration No.

SIN16354P

Indications:

Slinda is indicated for the oral contraception.

 

Product Name

COSENTYX SOLUTION FOR INJECTION IN PRE-FILLED UNOREADY PEN 300MG/2ML

COSENTYX SOLUTION FOR INJECTION IN PREFILLED SYRINGE 300MG/2ML

Active Ingredient

Secukinumab

Application type

NDA-2 and NDA-3

Product Registrant

Novartis (Singapore) Pte Ltd

Date of Approval

02/11/2021

Registration No.

SIN16358P, SIN16359P

Indications:

Plaque psoriasis

Cosentyx is indicated for the treatment of moderate to severe plaque psoriasis in patients 6 years and older who are candidates for systemic therapy or phototherapy (See section CLINICAL STUDIES)

Psoriatic arthritis

Cosentyx is indicated for the treatment of active psoriatic arthritis in adult patients when the response to previous disease-modifying anti-rheumatic drug (DMARD) therapy has been inadequate. Cosentyx can be used alone or in combination with methotrexate.

Axial spondyloarthritis (axSpA) with or without radiographic damage

Ankylosing spondylitis (AS)/ axSpA with radiographic damage

Cosentyx is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy.

Non-radiographic axial spondyloarthritis (nr-axSpA) / axSpA without radiographic damage

Cosentyx is indicated for the treatment of adult patients with active non-radiographic axial spondyloarthritis with objective signs of inflammation, as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) evidence who have had an inadequate response to, or are intolerant to nonsteroidal anti-inflammatory drugs (NSAIDs)

 

Product Name

HULIO SOLUTION FOR INJECTION 40MG/0.8ML IN PRE-FILLED SYRINGE

HULIO SOLUTION FOR INJECTION 40MG/0.8ML IN PRE-FILLED PEN

Active Ingredient

Adalimumab

Application type

NDA-2

Product Registrant

Mylan Pharmaceuticals Pte. Ltd.

Date of Approval

02/11/2021

Registration No.

SIN16360P, SIN16361P

Indications:

ADULTS

Rheumatoid Arthritis

Hulio is indicated for reducing signs and symptoms and inhibiting the progression of structural damage and improving physical function in adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more DMARDs. Hulio can be used alone or in combination with methotrexate or other DMARDs. Hulio, in combination with MTX, can also be used in the treatment of patients with recently diagnosed moderate to severely active rheumatoid arthritis who have not received methotrexate.

Psoriatic Arthritis

Hulio is indicated for reducing signs and symptoms of active arthritis in adult patients with moderate to severe psoriatic arthritis when the response to previous DMARD therapy has been inadequate. Hulio has been shown to reduce the rate of progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease and to improve physical function. Hulio can be used alone or in combination with DMARDs.

Ankylosing Spondylitis

Hulio is indicated for reducing signs and symptoms in adult patients with active ankylosing spondylitis who have had an inadequate response to conventional therapy.

Crohn’s Disease

Hulio is indicated for the treatment of moderate to severe active Crohn’s disease in adults to reduce the signs and symptoms of the disease and to induce and maintain clinical remission in patients who have had an inadequate response to conventional therapies, or who have lost response to or are intolerant of infliximab. For induction treatment, Hulio should be given in combination with corticosteroids. Hulio can be given as monotherapy in case of intolerance to corticosteroids or when continued treatment with corticosteroids is inadequate.

Ulcerative Colitis

Hulio is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies.

Plaque Psoriasis

Hulio is indicated for the treatment of adult patients with moderate to severe chronic plaque psoriasis who are candidates for systemic therapy or phototherapy and when other systemic therapies are medically less appropriate.

Hidradenitis Suppurativa

Hulio is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acneinversa) in adult patients with an inadequate response to conventional systemic HS therapy.

Uveitis

Hulio is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate.

PEDIATRICS

Juvenile Idiopathic Arthritis

Polyarticular Juvenile Idiopathic Arthritis

Hulio in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (pJIA), in patients 2 years of age and older, who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (DMARDS). Hulio can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate (for the efficacy in monotherapy see CLINICAL STUDIES). Hulio has not been studied in patients aged less than 2 years.

Enthesitis-Related Arthritis

Hulio is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy.

Pediatric Crohn's Disease

Hulio is indicated for reducing signs and symptoms and inducing and maintaining clinical remission in pediatric patients, 6years of age and older, with moderately to severely active Crohn’s disease who have had an inadequate response to conventional therapy.

Pediatric Plaque Psoriasis

Hulio is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapy.

Adolescent Hidradenitis Suppurativa

Hulio is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adolescents from 12 years of age with an inadequate response to conventional systemic hidradenitis suppurativa (HS) therapy.

Pediatric Uveitis

Hulio is indicated for the treatment of chronic non-infectious anterior uveitis in pediatric patients 2 years of age and older who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

 

Product Name

DOMIDE CAPSULES 50mg

Active Ingredient

Thalidomide

Application type

NDA-1: New chemical entity

Product Registrant

PHARM-D SINGAPORE PRIVATE LIMITED

Date of Approval

02/11/2021

Registration No.

SIN16362P

Indications:

DOMIDE in combination with melphalan and prednisone is indicated for the treatment of patients with untreated multiple myeloma≧65 years or ineligible for high dose chemotherapy.

DOMIDE in combination with dexamethasone is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue, for the treatment of patients with untreated multiple myeloma.

 

Product Name

CANHERA LYOPHILIZED POWDER FOR INJECTION 440MG

Active Ingredient

Trastuzumab

Application type

NDA-2

Product Registrant

Pharma To Market Pte Ltd

Date of Approval

25 Nov 2021

Registration No.

SIN16384P

Indications:

Metastatic Breast Cancer

CANHERA is indicated for the treatment of MBC patients who have human epidermal growth factor receptor 2 -(HER2)-overexpressing tumours.

  • as monotherapy for the treatment of those patients who have received one or more chemotherapy regimens for their metastatic disease

  • in combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease

  • in combination with an aromatase inhibitor for the treatment of postmenopausal patients with hormone receptor positive metastatic breast cancer, not previously treated with trastuzumab. This indication is based on data from one Phase III trial which studied the use of trastuzumab in combination with anastrozole (Clinical Efficacy). Experience with other aromatase inhibitors is limited.

Early Breast Cancer (EBC)

CANHERA is indicated for the treatment of adult patients with HER2 positive EBC.

  • following surgery, chemotherapy (neoadjuvant or adjuvant) and radiotherapy (if applicable) (see section pharmacodynamic properties).

  • following adjuvant chemotherapy with doxorubicin and cyclophosphamide, in combination with paclitaxel or docetaxel.

  • in combination with adjuvant chemotherapy consisting of docetaxel and carboplatin.

  • in combination with neoadjuvant chemotherapy followed by adjuvant trastuzumab therapy, for locally advanced (including inflammatory) disease or tumours > 2 cm in diameter (see sections warning and precautions and pharmacodynamic properties).

CANHERA should only be used in MBC or EBC patients who have tumours with either overexpression of HER2 or HER2 gene amplification as determined by an accurate and validated assay.

Metastatic Gastric Cancer (MGC)

CANHERAin combination with capecitabine or 5-fluorouracil and cisplatin is indicated for the treatment of adult patients with HER2 positive metastatic adenocarcinoma of the stomach or gastroesophageal junction who have not received prior anti-cancer treatment for their metastatic disease.

CANHERA should be used in only those MGC patients whose tumours overexpress HER2, as determined by an

accurate and validated assay:

· IHC2+ plus a confirmatory fluorescence in situ hybridisation (FISH) result, OR

· IHC 3+ result

 

Product Name

KERENDIA FILM-COATED TABLET 10 MG

KERENDIA FILM-COATED TABLET 20 MG

Active Ingredient

Finerenone

Application type

NDA-1 and NDA-3

Product Registrant

BAYER (SOUTH EAST ASIA) PTE LTD

Date of Approval

25/11/2021

Registration No.

SIN16387P, SIN16388P

Indications:

Kerendia, in addition to standard of care, is indicated to reduce the risk of sustained eGFR decline, end-stage kidney disease, cardiovascular death, non-fatal myocardial infarction and hospitalization for heart failure in adults with chronic kidney disease and albuminuria associated with type 2 diabetes.

*Evaluated via Access

 

Product Name

TEPMETKO FILM-COATED TABLET 225 MG

Active Ingredient

Tepotinib

Application type

NDA-1

Product Registrant

Merck Pte Ltd

Date of Approval

25/11/2021

Registration No.

SIN16386P

Indications:

TEPMETKO is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) harbouring mesenchymal-epithelial transition factor gene (MET)exon 14 (METex14) skipping alterations.

 

Healthcare professional, Industry member, Therapeutic Products
Published:

New Drug Approvals