Immix Biopharma (NASDAQ: IMMX)

Currency in USD

Last close As at 09/06/2023

USD2.03

0.06 (3.05%)

Market capitalisation

USD31m

Immix Biopharma’s lead asset, IMX-110, is being investigated in a Phase Ib/IIa study for the treatment of soft tissue sarcoma and a Phase Ib trial in advanced solid tumors in combination with the ICI tislelizumab. Immix also has a pre-clinical pipeline based on the TSTx technology.

With IMX-110 Immix is targeting the soft tissue sarcoma market, a rare cancer with c 13,000–16,000 new cases reported in the United States each year and limited safe and effective treatment options. IMX-110’s combination study may further expand the drug’s offering into new indications.

Scientist using protective robber gloves for handling substances and experiments

Sector

Healthcare

Equity Analyst

Soo Romanoff

Soo Romanoff

Managing Director - Head of Content, Healthcare

Key Management

  • Dr Ilya Rachman

    CEO

  • Gabriel Morris

    CFO

Balance Sheet

Forecast net debt (US$m)

15.1

Forecast gearing ratio (%)

N/A

Share Price Performance

Price Performance
% 1M 3M 12M
Actual (14.3) 2.0 (9.0)
Relative (17.5) (5.2) (12.7)
52 week high/low US$3.1/US$0.8

Financials

Immix Biopharma is a clinical-stage biopharmaceutical company focused on the development of its SMARxT tissue-specific platform producing tissue-specific therapeutics (TSTx). Its lead clinical asset, IMX-110, is being investigated for the treatment of soft tissue sarcoma, where interim results from its Phase Ib trial have, so far, demonstrated positive safety and efficacy profiles. Management intends to initiate a Phase IIa of the study in first-line soft tissue sarcoma in 2023. In Q422 Immix reported dosing of the first two patients in a Phase Ib/IIa study, investigating the use of IMX-110 in combination with tislelizumab in the treatment of solid tumors. We expect rolling data readouts across both studies throughout 2023. Immix Biopharma’s CAR-T therapy NXC-201 continues to demonstrate high response rates in multiple myeloma and AL amyloidosis from the Phase I/II NEXICART-1 study.

Y/E Dec Revenue (US$m) EBITDA (US$m) PBT (US$m) EPS (c) P/E (x) P/CF (x)
2021A 0.0 (1.4) (1.3) (35.91) N/A N/A
2022A 0.0 (8.2) (7.7) (55.49) N/A N/A
2023E 0.0 (10.9) (10.5) (71.81) N/A N/A
2024E 0.0 (14.4) (14.0) (93.33) N/A N/A

Subscribe to Edison

Get access to the very latest content matched to your personal investment style.

Sign up for free