Clinical-stage biopharmaceutical company Pulmatrix Inc (Nasdaq: PULM) announced on Wednesday that it plans to merge with Cullgen Inc, a privately-held company that specialises in targeted protein degradation for cancer and other diseases.
This merger will create a Nasdaq-listed entity focused on advancing Cullgen's proprietary uSMITE platform for the development of novel therapeutics. Cullgen has three degrader programs entering or about to begin Phase 1 clinical trials, targeting cancer and pain management.
The combined company, headquartered in San Diego, will have approximately USD65m in cash and cash equivalents upon closing, expected by the end of March 2025, to support clinical milestones through 2026. As part of the agreement, Pulmatrix will divest its iSPERSE-based migraine and other development candidates.
Upon closing, Pulmatrix shareholders will own approximately 3.6% of the merged entity, with Cullgen's shareholders holding 96.4%. Cullgen's Chairman and CEO, Dr Ying Luo, will lead the new company, which will continue under the name Cullgen Inc.
Cullgen's lead programs include CG001419, a first-in-class oral pan-TRK degrader for cancer and pain, and CG009301, a GSPT1 degrader targeting blood cancers. These therapies are expected to advance rapidly, with patient enrollment for CG001419's pain trial set for early 2025. Cullgen is also progressing several other degrader programs for cancer and autoimmune diseases, including a partnership with Astellas Pharma Inc.
Merck KGaA to acquire JSR Life Sciences chromatography business to expand Protein A capabilities
Bristol Myers Squibb to acquire Orbital Therapeutics for USD1.5bn to expand cell therapy portfolio
Celltrion launches AVTOZMA IV in the United States following FDA approval
OSE Immunotherapeutics forms strategic alliance with Inserm Transfert and Nantes University
Shoulder Innovations expands I-Series portfolio with launch of InSet 70 Humeral Stem
EMA recommends marketing approval of Alvotech's Gobivaz biosimilar to Simponi
Nanjing Leads Biolabs receives FDA approval of IND application for LBL-047
J & D Pharmaceuticals receives Orphan Drug Designation for JD-004
Hemogenyx reports positive safety and early efficacy data from third patient in CAR-T trial
Forte Biosciences highlights positive FB102 data in celiac disease at Tampere Symposium
Hemogenyx Pharmaceuticals partners with Made Scientific to advance CAR-T therapy
Onco3R Therapeutics receives Belgian regulatory approval for clinical trial of novel SIK3 inhibitor
ImmuPharma files patent for P140 'Immunormalizer' with precision diagnostic for autoimmune diseases
Coya Therapeutics wins FDA clearance to advance COYA 302 into Phase 2 ALS trial